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Purpose

• How to detect influenza in a lab?
• What kind of sample does the professor recommend for influenza rapid test?
• Do you recommend using the blood to detect the flu directly?
• Do you recommend using swabs to detect flu directly?
• What are the current methods of influenza detection?
• Do you have any suggestions for our fast screening products?

Process

• Generally, a bacterial culture is performed in a lab, and the whole process takes about 3 to 7 days.
• The general influenza samples have two forms, blood, and swab. The advantage of a blood sample is a lot amount at one time. The advantage of the swab is non-invasive.
• Dr. Chang recommended swab as the sample of our influenza rapid test. Since taking a blood sample needs to penetrate patients’ skin with needles, it is more invasive than taking a swab sample and less accepted by patients. Besides, drawing blood can only be conducted by professionally trained people, it isn’t good for promoting simple use. What’s more, a blood sample is valid only when there is viruses in the blood, or so-called viremia.
• Dr. Chang recommended that we design a kit that can test lots of pathogens and is user-friendly, which means everyone, even people who aren’t professionally trained, can use it. To know more about the technique he suggested we visit Adimmune Corporation.

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Form

Purpose

• Why are the control lines of rapid test kits designed by many companies different?
• Can we get patients’ samples from the Medical Laboratory in order to test our product? Or can we take our product to the medical laboratory to test it?
• How can we test our product?
• Why does the Medical Laboratory have to use a specific instrument to analyze the result of the rapid test? Can’t the result be read with naked-eyes?
• Why do they choose nasal mucus but serum as the sample for rapid influenza diagnostic tests?
• What is the mechanism of amplifying the signal of a sample in a rapid influenza diagnostic test?
• How high are the sensitivities of rapid influenza diagnostic tests nowadays?
• Is there anything of rapid influenza diagnostic tests that you want it to be improved?

Process

• Each company designs a different control line because they use different kinds of mice to produce antibodies. Just to make sure the sample can combine with the control line. Usually, they design various control lines, test and check the result, and choose the best one for production.
• The Medical Laboratory doesn’t keep samples after testing, and can’t give samples to us for testing our product, either. Without patients’ consent forms, patients’ samples can only be used for diagnosis. Biotechnical companies usually mix two different kinds of viruses as a sample for product testing at an initial stage. Too many different kinds of virus used at once is not recommended because it becomes hard to analyze the effect factors of the results. Types of viruses that will affect results are noted in Instruction manuals for doctors and laboratory scientists.
• We have to apply for experimental plans in order to get samples from the Medical Laboratory.
• The experiments to test products with different kinds of viruses must be taken in biosafety level-3 laboratories.
• Different medical laboratories of hospitals use different rapid influenza diagnostic tests.
• As for the data analyzing instrument we saw in the lab, it is used when the amount of the influenza virus in the sample isn’t enough, or for some fluorescence-used products that are hard to read with naked eyes. By using the instrument, there will be a standard for if patients are infected by influenza.
• Rapid influenza diagnostic tests always use samples collected from nasal mucus but serum because it is more difficult and more invasive to draw a patient’s blood than doing swabs, and the amount of the virus in nasal mucus is more than in blood, too. That is the reason why products nowadays seldom use samples collected from patients’ serum.
• When doing swabs, doctors will get into the patient’s throat as deep as possible to make sure they collect enough samples. The products nowadays seldom have a mechanism to amplify sample signals but they improve sensitivities by getting rid of the impurity. Some products contain enzymes to break down other bacteria or viruses to reduce interference. However not every company does so.
• The sensitivities of the products nowadays are not so good. Besides, many factors affect accuracy, for example, the ways doctors collect samples, the false negativity of products, or the disease process of patients is still at an early stage.
• It is impossible for patients to use the rapid influenza diagnostic test by themselves because the procedure of collecting samples must be done by well-trained doctors. Also, after using rapid diagnostic tests, patients still need to go see doctors and get treatments. It is worthless to let patients do the rapid test by themselves.
• We can try some ways to get rid of the impurity of other viruses or improve the sensitivities of our rapid test. It will benefit clinical medicine.

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Purpose

Process

• We saw a product called “Redeye”, which can detect invisible blood in our urine. It helps people discover their diseases such as colorectal cancer, kidney disease, bladder cancer earlier. It gives people awareness and makes them go to hospitals earlier for appropriate treatments. We found that early detection is very important in every kind of disease. People can use the device at home, which avoids the inconvenience of going to hospitals or getting invasive examinations. The company which produced “Redeye” wanted to combine their product with smart toilets and helped people examine their health with excreta. The device can connect to smartphones through wifi to get data.
• We saw many companies emphasized that their devices can detect many kinds of diseases or abnormal body function index. There was a product called “MSA—Blood” which can detect problems with a very small amount of patients’ blood. It can detect diabetes mellitus, liver function, cardiac function, kidney function, metabolism function and etc. Because of its convenience and fast analyze time, it can be used in some specific places such as clinics, care centers, nursing houses, ambulances, community health centers, schools, or rural areas. With these advantages, it might be possible to use it in every single family in the future. The market strategies and applications of this device are similar to ours.
• There were many posters and reports talking about the development of medicine, we were very impressed by one of them. The report was about the history of the development of infectious diseases in Taiwan, from SARS to influenza. The next trend of influenza is often predicted by WHO. But what can we do if WHO doesn’t predict right? The president of Min-Sheng General Hospital—Chiung-Lang Wang pointed out that if there is a shortage of the supplement of vaccines, or WHO predicts the wrong subtype of influenza for us to make vaccines, clinical workers and senior managers in hospitals will be under great pressure. In this situation, what hospitals and the public need are the technique of rapid diagnostic tests to help them figure out whether the disease is serious or slight. He recommended that faster and more efficient rapid diagnostic tests need to be developed.

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Form

Purpose

• Are aptamers able to act as antibodies in screening tests?
• How to select aptamers and to apply them to our rapid test paper?

Process

• Dr. Yu was developing screening tests with aptamers
• Yes, aptamers can perform the function of protein antibodies. In fact, they perform even better than antibodies since they are smaller in size.
• We apply SELEX(Systematic Evolution of Ligands by EXponential enrichment) to select the aptamers that have high affinity with our target proteins.
• Since Dr. Yu specialized in the screening tests of toxicant molecules, which are smaller than our target, influenza proteins, he wasn’t 100% sure whether aptamers would fit protein or not. However, Dr, Yu indicated that since the principle is the same it is supposed to work, and encouraged us to take a try.
• Aptamers are easier to process. If we want to have the color changed we can add nanogold or other substrates to the tails of aptamers.

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Form

Purpose

• We want to take the proteins of influenza as our target for SELEX. Could you give some advice to us?
• We find people often use HA and NP as influenza’s target proteins. If we want to produce them by ourselves, what recommendations or advice would you give us?
• How to produce proteins of high purification?

Process

• There are many complex chemical reactions in the human body fluid and it’s hard to predict. Aptamers have to bind to target protein when doing SELEX. Dr. Tsai recommended us using purified protein to do SELEX.
• Generally speaking, the water-soluble ability of HA is worse than NP. Dr. Tsai thought that to easily purify, using proteins that are better water-soluble and add His tag to the tail is a better choice. We can use Nickle columns to purify proteins.

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Purpose

• We have found through experiments that there was an unknown molecule with high molecular weight that appeared after SELEX. It seemed to be related to the template concentration, primer concentration, and the number of cycles. Why? How can we solve it?
• From our data, it is found that as the Template concentration or the number of PCR cycles increases, a by-product of about 100 bp would appear first and resulted in the ladder-like band. Then it evolved into a by-product with high molecular weight and resulted in the band gathering near the well that had a strong signal. How can we explain this situation?
(照片) Figure 1. Test of template conc. Condition (照片) Figure 2. Test of template and dNTP conc. condition (Wash compared with Probe) (照片) Figure 3. Experiment to find out the best template conc. condition of PCR. (照片) Figure 4 & 5. Test of PCR cycle number.

Process

• Template concentration or a high number of Cycles may has confused the Template and the Primer, resulting in incorrect copying or an unexpected secondary structure.
• The number of PCR cycles was too high. The general PCR condition after SELEX is 15 cycles. After conducting SELEX for many times, the product was relatively pure, and the number of cycles of PCR could be increased. It is recommended that the PCR part be tested first to find the most suitable conditions.
• The band of the product that appeared at about 100 bp may be the result of the double-stranded PCR product which hadn’t denatured, so the position of the band was higher than 87 bp which we expected. If there was no band, it represented that there was no product for PCR.
• Although the ladder-like by-products had occurred in the past, it hadn’t occurred that all by-products gathered at the top. However, a strong signal should be caused by its high molecular weight, not its volume.
• The professor recommended that we conducted SELEX experiment as follows:
  • Step: SELEX – PCR with Elution – Check by DNA page – Denature – Renature – Purify – Cryopreservation – Denature – Renature – SELEX
  • Control the number of PCR cycles, template concentration, and primer concentration during PCR to avoid the appearance of by-products.
  • Prior to each round of SELEX, using a Primer with beads to separate and remove the complementary sequence generated during the PCR process.
  • Quantify the PCR product before running SELEX to determine how much DNA is added to SELEX.
  • Increase the volume of PCR for subsequent testing and experimentation.
  • While denaturing, the recommended temperature is 95 degrees Centigrade and the recommended time is 10 minutes. While Renaturing (folding), it is recommended to slowly return the sample to room temperature from 95 degrees Centigrade instead of putting it on ice.
• The professor would start the specificity test after 5th round of SELEX. Under normal circumstances, the specificity will be enhanced successively. Usually, we can get the ideal result at the 7th to 8th round, and then we can conduct DNA sequencing. If conducting SELEX above 9-10 round, there may appear some impurities.
• Specificity test: Choose an unrelated protein (albumin) as a negative control, run the ELISA test with the proteins of the influenza A and B viruses, and confirm the result of DNA page after PCR.
• Affinity test: Conduct sequence dilution with Aptamer or Target. After getting a result of a binding curve, plot with Prism and get the KD value.
• The aptamer with good affinity should have a KD value below 10 nm, and an acceptable range for the value falls within 10-100 nm.

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Form

Purpose

• How does the government collect the data of the influenza subtypes every season? Which department collects and analyzes the data?
• What role does the rapid influenza diagnostic test play in the prevention work?
• How does the government know which subtype to make for vaccines next season?
• What is the countermeasure of the government for preventing influenza?
• In what situation should the clinic or hospital report the epidemic of influenza to the government? How do they report?
• Were the cases reported to the government diagnosed by using rapid influenza diagnostic tests, or according to their symptoms?
• Most of the rapid influenza diagnostic test nowadays have the problem of false negativities. Does it an issue for the government during the prevention works?
• Is the disease spreading map helpful for preventing influenza in Taiwan, or in developing countries?
• Where are the influenza virus during the rest period between every outbreak? Is it possible to stop the spreading of the virus during the rest period?
• If there is a product which can detect influenza more rapidly, correctly, and even cheaper, what impact will it bring to the public or the government?

Process

• Taiwan Centers for Disease Control (CDC) will collect the data from laboratories engaged by special arrangement. These laboratories in every city cultivate the virus and report the data to CDC. After CDC collects and analyzes the data, they announce the subtypes of influenza viruses that are prevalent each week. If there’s a rapid diagnostic test with higher accuracy and efficiency, it would help the government for the statistics of epidemiology.
• Most of rapid influenza diagnostic test products nowadays have up to 50% of false negativities. Doctors will take the result of these products as a reference, and consider other factors such as individual symptoms.
• There are many subtypes of influenza viruses, so it is hard to combine all of the subtypes in one rapid influenza diagnostic test. If only some common ones, it might be possible. It might have an impact on the type of influenza vaccine the government buys.
• WHO announces the subtype of influenza vaccines every season, and the government will take reference from it. Biotechnical companies provide vaccines globally, so it is hard to get specific types only for certain regions.
• The Department of Public Health monitors crowded places such as prisons, nursing houses, nurseries, schools. These places have to report if a cluster infection happened. A so-called cluster infection means that there are two or more infected cases each day. The reporting system is online and opens 24/7. After then, the Department of Public Health will conduct environmental disinfection and urge people to put on masks and even prescribe preventive medicine. Besides, the Department of Public Health will send propaganda to non-government institutions, reminding them to carry out preventing measures such as keeping windows open. The Department of Public Health will provide them a checklist to help them make sure that they are prepared for the upcoming outbreak.
• For general non-government institutions, the cases reported have to be diagnosed by doctors. Doctors take the results of rapid influenza diagnostic tests as a reference, combined with patients’ symptoms to make diagnoses.
• The disease spreading map is not useful for the prevention works in Taiwan. For the one-day-life circle in Taiwan, the virus could spread around Taiwan in a very short time. For the developing countries which their traffic is inconvenient or with broad territories, it may be helpful.
• During the rest period between each outbreak, influenza viruses don’t disappear,. However, they exist in human bodies. It is hard to find all of the influenza viruses during the rest period and eliminate them.
• If there is a product that can detect influenza more rapidly, correctly, and even cheaper, the clinics will be willing to buy so they can know if the patients are infected by influenza in a more efficient way. The government can also start their prevention works earlier and additionally prevent the widespread of influenza viruses.

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Form

Purpose

• Rapid diagnose tests could hardly avoid the problem of false negativities. In this situation, what is the position of clinical application?
• What kinds of certification should a successfully developed product get before it is launched in the market?
• How do general laboratories manufacture and market outsource?

Process

• Dengue fever is a major project for the prevention of infectious diseases in Taiwan every year. AsiaGen Corporation developed the product “Dengue fever NS1 rapid diagnose test” and it is the only product certificated in Taiwan now. The product can detect 4 types of dengue fever at the same time. While using RT-PCR, it needs 6 hours to get the result, this product only takes 30 minutes to examine dengue fever. It is a very convenient product, consuming little time and saving spaces. The product has 98-99% of sensitivity and has low false negativities. However, it is only for front line examination use. Dengue fever has to be confirmed by rTP—ELISA.
• We asked them about how they confirm the sensitivity. They said they have tested it by the dengue virus in their laboratory. Besides, they suggested us test our product with the whole influenza virus.
• They suggested we visit the Innovation Incubation Center of our school, for the questions such as applying for patents.

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Form

Purpose

• What is the mechanism of your(TaiGen) new influenza medicine—TG1000? How does it function as a medicine and a vaccine at the same time?
• In the industry of influenza medicine, what aspect do the biotechnology companies focus on? What is the present situation of the influenza market? Why does TaiGen choose influenza as the subject to develop?
• How do biotechnology companies estimate the potential and prospect of a newly developed product? What aspect should be noticed?
• Can aptamers be applied to medicine?

Process

• Mr. Chen said that the mechanism of their new medicine—TG-1000 is Cap-snatching. It inhibits the duplication of influenza viruses and has shown well result on animal tests. It resists Type A and B and avian influenza H7N9 infection. Moreover, the validity period of the medicine lasts for 72 hours, which is better than Tamiflu. There isn’t only one molecule of the virus in one cell, so medicines have to reach a certain concentration to have a function. The viral molecules will combine with the medicine through random collision. By measuring the medicine's inhibition constant (IC50) or so-called binding constant can let us know their affinity to viruses.
• The influenza virus often infects lung cells, however, the concentration of the medicine in the blood doesn’t represent the same as in the lung. It is important to prove that the concentration in both places is proportional. Also, confirming that whether the medicine can exactly achieve the goal is very important.
• The product is design as an oral medicine for easier taking in. Different diseases have different consideration, for example, intravenous injection make medicine spread faster in body but oral medicine is more convenient for patients to take in.
• Besides providing community immunity, the advantage of their product is its slow metabolism rate. It keeps the effect even longer than a week, so it doesn’t need to be taken earlier before infection like a vaccine, and the effect is also much better than the vaccine.
• The limitation of the medicine is that the safety range of the dosage is narrow. If a child showed resistance to some other flu medicine, doctors can’t increase the dosage for the concern of safety. Although TG100 hasn’t passed a human test, the result of an animal test showed that the dosage can be increased.
• The reason why they choose to develop influenza medicine is that there are 3 to 5 million people affected by influenza annually, and Tamiflu, the flu medicine most commonly used, has many limitations needed to be improved.
• If technology advanced more in the future, it is possible to design an antibody by just knowing the structure of the protein of a virus. With gene sequencing, we are able to compare the similarity between different viruses similar and apply the same medicine to similar ones, which reduces the cost of the process to develop new medicines.
• As for applying aptamer to medicine, Mr. Chen agreed with our idea. He said medicine is not restricted to only a specific type. He emphasized that collecting data is very important.

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Form

Purpose

Influenza and Aptamer

• If we would like our rapid diagnostic test product to help the government predict epidemiological trends, will it make the product more valuable if it can distinguish subtypes?
• If our product could provide not only AB subtype but also information about the time and places infection occurred. Is it more helpful for predicting epidemiological trends?
• Is it possible to predict the trends of the disease spreading after an outbreak?
• Does our product help increase the effectiveness of making vaccines?
• At Asian Health Exhibition, we met TaiGen Biotechnology and we knew that they had produced a new drug called TG1000. They claimed that it has a long-term half-life, so it has a preventive effect on flu. Aptamers also have the property of inhibiting virus invasion. How can we apply the feature to make a therapeutic and preventive medicine?
• Is it feasible to apply aptamers to vaccines?
• Is it feasible to apply aptamers to automated wafer technology?

Marketing and Commercializing

• What kinds of standards are required for a product to put on the market? How are these standards usually been set?
• Who will be the target groups of our product on the market?
• If we want to develop a rapid diagnostic test product with aptamers in the future, is it possible to be put on the market?
• Is it possible that our product replaces antibody type of rapid diagnostic tests in the future?
• How can we obtain market analysis data? How to judge the professionalism of data?

Process

Influenza and Aptamer

• If our purpose is to predict epidemiological trends, of course, distinguishing subtypes are useful. Providing more detailed information such as time and places are also helpful since the epidemic data of Taiwan is one of the resources WHO make subtypes prediction with.
• Because there is no specific treatment for type A and type B, it won't help much on disease spreading after the flu outbreak, but it is helpful for WHO to understand the world epidemiological trends, especially if it can distinguish subtypes.
• The idea of applying aptamers to therapeutic is good. Aptamers are macromolecules and can block the target protein from viral invasion. If we choose HA as our target, it is important to follow its evolvement because HA changes every year.
• As for the idea to apply aptamers to preventive medicine, peptide vaccines. A peptide vaccine is any peptide that serves to immunize an organism against a pathogen. They are often synthetic and mimic naturally occurring proteins from pathogens. The researchers said the immune response of human bodies is so complicated that the development of the vaccine would be difficult. Most of the vaccines were mostly been found accidentally.
• The idea of applying aptamer to automated wafer technology is very good, but we need a more detailed operating mechanism to know if it is feasible. We can imagine a scene and think of the design, such as applying automated wafer technology to a microrobot or an aerial camera.
• We have to provide data about the processing speed. Since the subtypes change quickly, it is vital that the process becomes faster.
• We can use “Hai” to perform blood cell coagulation experiments first, and we can get the results in a few hours.
• Start with influenza, in the future, we can apply it to other targets such as Enterovirus 71.

Marketing and Commercializing

• It is necessary to confirm whether the quality of the raw materials produced is always consistent. The storage period and the storage environment need to be supported with data. Besides, it is necessary to test whether the data measured by different people on different days are equal. The specifications of each component should conform to the standard. It is vital to set QA and QC methods according to our products.
• Mainly doctors are our target groups, they care about accuracy and price. The key point is to choose a good target for this product. The advantages of our product over existing ones are price, stability, sensitivity. For the companies, it isn’t attractive if it only distinguishes A or B type, but it would be very attractive for distinguishing subtypes. The government may cooperate with companies if he wants them to report subtypes, and the market will become bigger. Subtypes of influenza change quickly, which means that the efficiency of producing rapid diagnostic test becomes so important that it can distinguish various subtypes.
• It isn’t difficult for our product to pass the regulations and for manufacture. It is possible for this technique to enter the market.
• If there are advantages in price and accuracy over the existing antibody type products, it is affirmative that our product replaces them someday.
• We can find some companies, teams or papers doing research about market analysis or buy the data from companies. Besides, we can ask foreign companies.
• It is vital that we pay attention to the regulatory issues when modifying a product, and to comply with government regulations while doing research and developing.
• We have to make a substantial comparison figure for products used nowadays. If the price of us is lower and easier to manufacture than antibodies-type rapid tests. The existing products will be replaced by aptamers-type ones in all aspects.
• We can consider more innovative ideas for further application such as hand lotion.

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Purpose

Process

• eNano Health Limited--Kiss & Tell—1st ever Saliva-Based Glucose Monitor: The product takes saliva as a sample instead of blood to examine glucose.
• eNano Health Limited--Manage Health Risk Before Feeling Sick: The product let users know their eating conditions through convenient testing tools. If there is a risk of their health (such as a high-risk group of diabetes), the users can eat the food developed by the company “eNANO P4 Food”. Users can use the App to share data with physicians and track their physical condition at any time to achieve health management.
• Helios Bioelectronics Inc. --Disease detection platform: The probe is coated on an electronic wafer, and the sample is reacted with the wafer, and then an electronic sensor is used to know whether a disease is present or not. The sample can be nucleic acids, proteins or cells. Through real-time digital results, combined with big data analysis, it can assist clinical diagnosis to achieve precise medical goals. The probes are coated on the electronic wafer by using covalent bonds, and they are well designed and were highly specific. Because the cost of the wafer is high and the entire wafer can’t be full of probes, so a dot distribution is required. In addition, the wafer is currently not reusable. The product directly relies on the change of the electrical signal to know the result (coloring is more troublesome).
• Papivax Biotech Inc.--HPV therapeutic vaccine: The HPV vaccine currently on the market is a preventive vaccine. However, the incubation period of HPV is long. If the abnormality is detected but not reach the level of becoming cancer, the patient will have to endure this unknown suffering for a long time (about 5~10 years). Therefore, the newly developed therapeutic vaccine, using prime-boost therapy, can break into the DNA fragment of HPV, activate T cells through cellular immunity, attack infected cells, and prevent infection from spreading. We asked the researchers of the company some questions about how to avoid DNA degradation. They said it is difficult to know and they have observed through the amount of virus in the course of treatment. Then we asked how to confirm that the DNA injected to human bodies won’t become another pathogen. They said these DNAs do not enter cells but only induce T cells.
• La vida Tech—WaCare: The product plays a role in preventive medicine. It helps users connect with friends and relatives, hospitals and health education units by entering various indicators of a body to form a network of care. If there are any abnormalities, the users’ friends, relatives or physicians can immediately know the situations and remind them. As for online health consultation and remote medicine, if users have health-related concerns, they can get professional and correct information through consultation with dietitians, pharmacists, and doctors.
• Studio1labs—Smart Sheet: Through the sensing elements inside the sheets, the heartbeat, breathing, posture changes of a patient lying on it are detected. Chronic disease and the condition of a postoperative patient can also be tracked.
• Guzip Biomarkers Corporation—Cervical cancer detection paper: By detecting the methylation of DNA on the uterine surface, the product can determine whether there is a potential risk of cervical cancer.

Feedback

• eNano Health Limited--Kiss & Tell—1st ever Saliva-Based Glucose Monitor: We started to think of the possibilities of developing our product as using saliva as the sample.
• eNano Health Limited--Manage Health Risk Before Feeling Sick: The idea of this product is very interesting and could be a business model for a combination of atypical forced marketing kits. In addition, the idea of App management seems to be applicable to our influenza detecting product.
• Helios Bioelectronics Inc. --Disease detection platform: We discussed the possibility of applying aptamer to an air purifier, the researchers of the company thought it an interesting idea. We could apply an electronic wafer to our air purifier design. The principle is that when the target substance in the sample is attached to the probe (aptamer), it changes the electronic arrangement of the wafer and further changes the electrical signal. In order to make the wafer reusable, we then think about whether there is any way to get the attached object to fall off the probe. The probe is connected to the target by hydrogen bonding, and the probe and the wafer are connected by covalent bonds. There should be other methods.
• Papivax Biotech Inc.--HPV therapeutic vaccine: We came up with an idea of applying our product to a therapeutic vaccine. The company's products correspond to the concept of our therapeutic vaccine. The therapeutic vaccines of our works also include the part of injecting DNA (aptamer) into bodies, but the principle is different. Our concept is inhibiting viruses to infect cells by binding to the viruses. Their product injects DNA into human bodies. It helped us figure out the problem that whether aptamer will degrade in human bodies and whether it will become another risk of infection. After the interview, we started to study how to stabilize the DNA injected into human bodies and how to enhance the signal.
• La vida Tech—WaCare: We asked the possibility of introducing our product to their App. The results of our product can be determined by naked eyes and it doesn’t require special equipment. Small-scaled hospitals, clinics, and even kindergartens can use our product and get results directly. However, since the accuracy of influenza screening is not very high, there may be false-negative results. If our product integrates with the app, users can get diagnosed through the results of our product and symptoms. They can also get medical advice and information. We thought it a great opportunity to cooperate with the company and develop an App. It was a precious opportunity to know different products in the market. There were many inspiring ideas at this conference. We came up with more concepts that we can apply to aptamers after attending this conference. We not only inspected and studied from other newly developed products but we also confirmed some of our idea through the discussion with the entrepreneurs.

Form

Purpose

• Is there any legal issue related to our product that we should be noticed?
• Before conducting technology transfer, what should we notice?
• What kind of patent right is recommended for us to apply?

Process

• All new developed medical equipment should get medical equipment licenses from the government. We had to notice that which grade our product was. Our product should meet the regulations of that grade.
• We have to submit information about our product such as the instruction manual, materials, structure, function, use. Besides, we have to fill out an application form. The manufacturers had to submit a Medical Device License and Good Manufacturing Practice License.
• After conducting technology transfer to manufactures, there might be serious problems to notice that sometimes the technicians of manufactures might not be able to understand the principle of the product so they can’t find out the best way to produce on a large scale.
• Different companies would have different business strategies. Some companies focus on developing new products, some focus on producing, some focus on marketing. There are also some companies that run the whole process.
• Because our product would be known to the public, it is better to apply the patent right first. It is often recommended that the researchers started to fill out the forms of the patent right and submit it first because the procedure will last for at least a year.
• There is another kind of patent right which the review procedure would be shorter than the general one. However, the protection of the patent right would only last for 10 years, which is much shorter than the general one. Besides, we have to record all the details of our product and technique. Otherwise, other people can imitate the product easily.

Feedback

Form

Purpose

• What roles do technology transfer companies play while producing rapid diagnose test products? What is the characteristic of External Material Company?
• How to distribute the profit of technology transfer? How to assign a different type of technology transfer (exclusive license or not)?
• How long does it take from receiving the technology and producing the final product?
• We would like to introduce our research and the issue we have confronted and ask for recommends.

Process

• External Material Company can meet the clients’ requirements, providing monoclonal antibodies in a specific way. The company is now developing antibodies for detecting vector viruses and infectious diseases. Using their product--Serotype-specific Dengue NS1 Antigen Rapid Test Strips, which is easy to use, can detect NS1 protein in whole blood. It gets correct and detailed information with only a little amount of sample, which helps the government and medical institutions to identify the virus and provide more information about dengue fever. The product can also distinguish four types of dengue fever, which can be used for data statistics and assists airport customs to know whether passengers are infected by dengue fever in a faster way. Traditional methods can’t distinguish the subtypes of dengue fever. The sample has to be sent to laboratories to analysis, which might take one day. The product shortens the processing time to only 30 minutes.
• Because the technique was provided by the government, and the government doesn’t give an exclusive license, so what External Material Company gets was a non-exclusive license. It means that if other companies want to use this technique, they can also get it.
• In fact, aside from the antibody, the key point of producing a rapid diagnostic test is the formulation of the buffer. How to avoid cross-reaction is very important.
• As for distributing the profits, the External Material Company paid money for the technique to the laboratory first. If the company gets the certification, they would give a reward. If they sell the product to other countries, they have to pay a proportion of money back to the laboratory.
• External Material Company could have accomplished the designation of the product in one year since they had made similar products before and applied the experiences to the Dengue fever test kit. Without related experiences and professionals, it may take at least 3 years.
• The characteristic of External Material Company is they provide antibodies by themselves, which reduces cost and they don’t need to worry about the shortage of antibodies in the market.
• About the issue of DNA sequencing that our team is confronting, Tang Ph.D. gave us some suggestions. The first is about how to make confirmation after DNA sequencing. Generally, antibodies and antigens can be amplified with ELISA, but the signal of the aptamer is very small which is closed to the background level. Tang Ph.D. suggests we use some simulation software such as Gene Duck, Auto Duck®, and Discovery Studio. We can put the aptamer sequences in these softwares and simulate if the aptamer can combine with the protein. Some laboratories thought that SELEX is hard to conduct so they simply use softwares to find our the aptamers they want and synthesis the sequence.

Feedback

Form

Purpose

• While conducting the experiment, what kind of legal or ethical issues should be noticed?
• What issues will we face if our rapid diagnostic test product gets into the market?
• What kind of issues or challenges will we face if our therapeutic vaccine gets into the market?
• If our rapid diagnostic test product or therapeutic vaccine gets into the market, what laws should we notice? What ethical issues or challenges we have to confront?
• What is the universal cognition of the public for the issues of genetic modification and gene processing? Is the acceptance level high?
• For the government, is there any concern about public safety?

Process

• Institutional Review Board (IRB) is a type of committee that applies research ethics by reviewing the methods proposed for research to ensure that they are ethical. While IRB reviewing applications, the committee members will check if our experimental procedures comply with laboratory safety specifications. We had to take notice of laboratory safety specifications.
• Rapid diagnostic tests belong to the category of medical equipment. Before getting into the market, it has to pass IRB and the examination of the Taiwan Food and Drug Administration (TFDA). Before passing IRB, it is still at the testing phase. In the future, it will have to conduct clinical trials, documents of the experimental designation, procedure and the environment should be submitted to IRB. Moreover, there will be a Sociologist examining whether the clinical trial is ethical.
• The issue which our products would confront is whether our product could get into the market before the outbreak. Other issues are that the advantages of detecting subtypes would be useless if WHO predicted the wrong subtypes with the help of our product.
• As for the therapeutic vaccine, it belongs to the category of medical equipment. It has to conduct clinical trials and pass the examination of TFDA. Besides, therapeutic vaccines belong to the third level of medical equipment.
• Before our product getting into the market, there would be many issues about patents that we should take notice of, including the experimental procedure and technique.
• For rapid diagnostic tests, the ethical issues we should be noticed are that if the product is safe and effective and if the cost of production is too much. As for therapeutic vaccines, they have to conduct clinical trials and go through four phases. First is to make sure it is safe by testing the safe dosage. Second is to make sure it is effective by finding some patients to test it. Third is large-scale testing by finding 2000 to 3000 patients to test the effectiveness. Forth is long-term monitoring for 5 to 10 years.
• While conducting the clinical trials, we have to obey four principles, which are respect for autonomy, non-maleficence, beneficence, and justice. Moreover, issues such as products after genetic modification being exposed to the environment should be noticed.
• Most people know that genetically modified food won’t be harmful to the human body. Most of the misunderstandings are driven by the media. The government doesn’t request companies to mark that they are genetically modified food.

Feedback

Form

Purpose

• We had searched for some information and knew that the government will randomly inspect some chicken farms to find if they have poultries infected by Avian Influenza. How does the government inspect poultries?
• Is the detecting method nowadays able to prevent the spread of Avian influenza effectively?
• Is it possible to replace the method used nowadays with rapid diagnostic tests?
• Are rapid diagnostic tests useful for examining the chicken?
• Is there any flaw in the prevention work of Avian influenza?
• Is it useful to prevent the spread of Avian influenza by early detection?
• What measures does the government use to know if migratory birds are infected by Avian influenza?
• Is it possible to apply our product to the detection of if migratory birds are infected by Avian influenza?

Process

• The government usually inspects the poultry farms that are more willing to be inspected. There are many poultry farms that often refuse their random inspection, which might be a risk to the public. The research institute often checks the poultry farms by taking the sample of some poultries and take the sample to the laboratory to analyze them through RT-PCR.
• There are many poultry farms that are not willing to be inspected. And for those farms agreed, not all of them would be inspected. The government visits some of the farms, collecting samples, and send them to the laboratory to analyze. The problem of preventing work is not the detecting methods but that many poultry farms are not included in the prevention works.
• RT-PCR is a precise way to examine if there is a virus of Avian influenza in samples. Using a rapid diagnostic test cannot get an accurate result. Besides, examining all of the poultries with rapid diagnostic tests is time-consuming and unnecessary. It is more efficient to examine with RT-PCR.
• Aside from the problem that many poultry farms are not involved in Avian influenza prevention work, the problem of self-inspection of Avian influenza worth noticing. The government set up compensation for the poultry farms affected by Avian influenza. However, many farmers are not willing to report to the government that their poultries are inflected by Avian influenza. If they do so, the government will cull all of the poultries and the compensation is not enough to cover their losses. This results in the problem that only little farmers would report to the government about epidemics.
• It might be useful if there is a method that can help the government early detect epidemics of Avian influenza. It is important that all the poultry farms are included in preventing works. It helps the government master the situation and make responses in advance.
• As for migratory birds, the method they use to detect Avian influenza is that some experts collect samples of migratory birds and send them to the research institute to analyze. Because the samples are only of little amount, they often analyze them through RT-PCR. If they find Avian influenza in the sample, they will give the information to the media and remind other farmers to be aware of it.
• A rapid diagnostic test is not that useful for detecting Avian influenza in migratory birds because the sample is not much and they have to make sure that the result is correct.

Feedback

Form

Purpose

• How to detect influenza in a lab?
• What kind of sample does the professor recommend for influenza rapid test?
• Do you recommend using the blood to detect the flu directly?
• Do you recommend using swabs to detect flu directly?
• What are the current methods of influenza detection?
• Do you have any suggestions for our fast screening products?

Process

• Generally, a bacterial culture is performed in a lab, and the whole process takes about 3 to 7 days.
• The general influenza samples have two forms, blood, and swab. The advantage of a blood sample is a lot amount at one time. The advantage of the swab is non-invasive.
• Dr. Chang recommended swab as the sample of our influenza rapid test. Since taking a blood sample needs to penetrate patients’ skin with needles, it is more invasive than taking a swab sample and less accepted by patients. Besides, drawing blood can only be conducted by professionally trained people, it isn’t good for promoting simple use. What’s more, a blood sample is valid only when there is viruses in the blood, or so-called viremia.
• Dr. Chang recommended that we design a kit that can test lots of pathogens and is user-friendly, which means everyone, even people who aren’t professionally trained, can use it. To know more about the technique he suggested we visit Adimmune Corporation.

Feedback

Form

Purpose

• How to detect influenza in a lab?
• What kind of sample does the professor recommend for influenza rapid test?
• Do you recommend using the blood to detect the flu directly?
• Do you recommend using swabs to detect flu directly?
• What are the current methods of influenza detection?
• Do you have any suggestions for our fast screening products?

Process

• Generally, a bacterial culture is performed in a lab, and the whole process takes about 3 to 7 days.
• The general influenza samples have two forms, blood, and swab. The advantage of a blood sample is a lot amount at one time. The advantage of the swab is non-invasive.
• Dr. Chang recommended swab as the sample of our influenza rapid test. Since taking a blood sample needs to penetrate patients’ skin with needles, it is more invasive than taking a swab sample and less accepted by patients. Besides, drawing blood can only be conducted by professionally trained people, it isn’t good for promoting simple use. What’s more, a blood sample is valid only when there is viruses in the blood, or so-called viremia.
• Dr. Chang recommended that we design a kit that can test lots of pathogens and is user-friendly, which means everyone, even people who aren’t professionally trained, can use it. To know more about the technique he suggested we visit Adimmune Corporation.

Feedback