Tuesday, May 6, 2014

Electrical Modstandstomografi Tomography is a medical imaging technique that has been around for de

Tomography for the future
Electrical procestomografi provides three-dimensional images of protein synthesis and separation in chromatography columns. It is one of the few methods that can evaluate the effectiveness of packed columns in situ. Read the original article here This article has been published in Danish Chemistry No. 6/7, 2011 and can be read without illustrations, structures and equations below. See related articles below.
In the preparation and purification of the proteins are often used packed columns. The yield depends on the flow conditions h2co3 through the column, and there are column material h2co3 often very expensive. So far it has been difficult to assess the quality h2co3 of the packing of the material h2co3 and of the column useful life. To get a better understanding of how packed columns h2co3 operate and to increase their efficiency, ITS has worked for several years with electrical tomography in packed columns. The results of the studies carried out in collaboration with two customers in the pharmaceutical and biotech industry are briefly summarized here.
Electrical Modstandstomografi Tomography is a medical imaging technique that has been around for decades in the form of CAT Scan (Computed Axial Tomography) used for imaging. The original h2co3 X-ray methods have been developed, for example. NMR (Nuclear Magnetic Resonance) and PET scan (positron emission tomography). In the 1990s, a number of universities (particularly h2co3 Leeds and Manchester) research into using these techniques to industrial processes. The work showed that the best industrial practices are electrically modstandstomografi and electric kapacitanstomografi. The sensors are robust and easy to install (usually consist of an electrode array located on-site at the process plant). The computer unit that provides data processing h2co3 is relatively small, h2co3 making it possible to measure a wide range of processes in various industries within Farma, Petrochemicals, Mineral Mining, Pulp & Paper, Food and Beverages. The measurements can be performed directly on the process on an industrial scale, and one does not, as is generally the case for X-ray, NMR or optical h2co3 methods to conduct the measurements in the laboratory. Electrical modstandstomografi, or to use the English term and abbreviation ERT (Electrical Resistance Tomography), usually obtained from the fitting of a ring with electrodes on the surface of a pipe or vessel. Normally, a total of 16 electrodes, but also 8 or 32 can be used (like other forms as probes and channels). An AC potential difference is applied between two electrodes and an electric field. When the reference area disturbed areas with either high or low conductivity change field lines. Crushing by high conductivity, and is repelled by the low conductivity. This changes the potential difference measured by the adjacent edge, as shown in Figure 1b, which are red and blue areas, respectively. high and low conductivity. Thus, changes in the composition of a process volume h2co3 affect the measurements at the edge. The challenge now is that all the measurements h2co3 from the periphery of the volume to be further processed to determine how the conductivity to disperse the material within the container, wherein the potential differences were measured. There are many ways to solve this problem. This report used two approaches based on commercially available software from ITS Industrial Tomography Systems (see www.itoms.com)
The imaging of the packed columns, the images 5 of Figure 2 shows the transition between h2co3 two buffers in a flow through the column. The conductivity varies from 10 to 20 mS / cm. Data was collected by the measuring electrodes 128 located on the circular arrays 8, 16 each provided with electrodes in direct contact with the medium in the column. The column performance can be tested by a number of separations, giving h2co3 an overall assessment h2co3 of the column mode.
Oligonucleotide synthesis A technique for the synthesis of oligonucleotides is to build short chains group by group. While this may require up to 80 steps, it is a very accurate method. The yield of the process is critically dependent on the efficiency h2co3 of each stage, which in turn is dependent on the packed column performance, since it acts as a matrix in which the chains built up. A tomografisensor with 4 rings with hver16 electrodes were embedded in a column, and the synthesis of each step was monitored.
Conclusion The studies described indicate the potential of ERT as a means to visualize the flow through the packed chromatography columns. With the very high investment required for these processes, the value of the finished products and high production costs, offering tomography a better understanding of the processes paths and opportunities to enhance h2co3 both the control and productivity, respectively, protein synthesis and separation.
Thanks to our partners h2co3 ITS would like to thank Genzyme and PASG, Pfizer, which has hosted two of the studies and has provided both process equipment like material available

Monday, May 5, 2014

The content of the leaflets of this website is informative and does not replace the original prospe


The content of the leaflets of this website is informative and does not replace the original prospectus (which is included in the product box). If you have questions, contact your doctor or pharmacist.
PACKAGE LEAFLET: INFORMATION FOR THE USER CellCept 500 mg tablets simple sugars mycophenolate simple sugars read this leaflet carefully before you start taking this medicine. Keep this leaflet. You may need to read it again. Ask your doctor or pharmacist if there is more you want to know. This medicine has been prescribed for you personally. You should not pass it on to others. It may harm them, even if they have the same symptoms that you have. Talk to your doctor or pharmacist if any of the side effects gets serious, or you notice any side effects not listed here. In this leaflet: 1 Effect and use 2 What you need to know before you start taking CellCept 3 How to take CellCept 4 Possible side effects 5 How to store 6 Further information 1 AND USE Immunosuppressants. CellCept tablets are used to prevent simple sugars the body from rejecting a transplanted kidney, heart or liver. CellCept is used together with other medicines known as ciclosporin and corticosteroids. 2 BEFORE YOU BEFORE YOU TAKE CELLCEPT Do not take CellCept: simple sugars If you are allergic (hypersensitive) simple sugars to mycophenolate mofetil, mycophenolic acid or any of the other ingredients of CellCept. If you are breastfeeding. Take special simple sugars care with CellCept: You should inform your doctor immediately: If you experience any signs of infection (eg. Fever, sore throat), unexpected bruising and / or bleeding. If you have or have ever had problems with your digestive system, for example. ulcer. CellCept reduces your body's simple sugars defense mechanisms. For this reason, there is an increased risk of skin cancer. Therefore you should limit your exposure to sunlight and UV light by wearing protective clothing and using a sunscreen with a high protection factor. Taking simple sugars other medicines Please tell your doctor or pharmacist if you are taking or have recently taken. This includes medicines obtained without a prescription. If you answered yes to any of the following questions, please talk with your doctor before you start taking CellCept: Are you taking any medicines simple sugars containing: azathioprine or other immunosuppressive agents (which simple sugars are sometimes given to patients after a transplant operation ), cholestyramine (used to treat patients with high blood cholesterol), simple sugars rifampicin (antibiotic), antacids, phosphate binders (used in patients with chronic renal failure to reduce the absorption of phosphate) or other drugs (including prescription drugs) that your doctor does not is aware of? Going vaccines (live vaccines)? Your doctor will advise you about which vaccines you may use. Taking CellCept with food and drink: Taking food and drink has no influence on your treatment with CellCept. Pregnancy and breast-feeding: Do not take CellCept if you are breastfeeding. Do not use CellCept during pregnancy unless clearly indicated simple sugars by your doctor. Your doctor should advise simple sugars you about using contraception before taking CellCept, while taking CellCept, and for 6 weeks after you have stopped taking CellCept. This is because CellCept may cause miscarriage or harm your unborn baby, including problems with development of the ears. You should immediately tell your doctor if you are pregnant or nursing, or if you are or intend to become pregnant. Driving and using machines: There is no evidence that CellCept affect the ability to drive and use machines. 3 HOW TO TAKE CELLCEPT Always take CellCept exactly as prescribed. If in doubt, ask your doctor or pharmacist. The usual dose is: Kidney Transplant Adults: The first dose will be given within 72 hours after the transplant. simple sugars The recommended daily dose is 4 tablets (2 g of the active ingredient) taken as two separate doses. This means that you have to take 2 tablets in the morning and 2 tablets in the evening. Children (2-18 years): The dose depends on the child's size. Your doctor will decide the most appropriate dose based on body surface area (height and weight). The recommended dose is 600 mg/m2 twice daily. Heart Transplant Adults: The first dose will be given within 5 days following the transplant. The recommended daily dose is 6 tablets (3 g of the active ingredient) taken as 2 separate doses. This means that one should take 3 tablets in the morning and 3 tablets in the evening. Children: The use of CellCept in pediatric heart transplantation is not recommended as there is no data. Liver Transplant Adults: The first dose of CellCept oral given 4 days after transplantation, and when you are able to take the medicine

Sunday, May 4, 2014

Atom Transfer Radical Polymerization Within the last eight years, a number of controlled free radic

Controlled free radical polymerization - a world of new possibilities acid
A variety of commercially available plastics based on polymers made by free radical initiated polymerization. This process does not give good control of chain length and structure as the growing polymer chains are constantly undergoing various non-verifiable termination or transfer reactions. If you want polymers with well-controlled chain lengths, special chemical functionality such. at the chain ends or in well-defined blocks, has so far been used anionic or cationic living polymerization techniques. The living polymerisationskoncept means that the polymeric structure acid can be extremely well controlled by well-defined, rapid initiation, propagation and termination without conservation of the active, ionic chain end, when all of the monomer has reacted. Subsequently, block copolymers can be prepared by the addition of a new monomer. Technically, it is very difficult, and only a very limited number of monomers can be used in this way.
Atom Transfer Radical Polymerization Within the last eight years, a number of controlled free radical techniques, however, have been developed. The main innovation is that they are usually unavoidable transfer and termination reactions, acid which occur in the free radical polymerization, can be suppressed almost completely. This is due to the growing chains in the greater part of the polymerization process is in a quiescent state for the momentary being activated acid to a polymer chain radical, adding one or more monomers and then return to the off state. For Atom Transfer Radical Polymerization acid (ATRP) [1] of styrene this is illustrated in Figure 1, the reversible redox process of polymer radicals are formed, acid catalyzed by a copper complex undergoes a one-electron oxidation, while the halogen (here bromide) simultaneously transferred from the dormant polymer acid chain end. Deaktiveringshastighedskonstanten, acid kd, however, is 108 times greater than aktiveringskonstanten, ka, so the resting state is restored after a few monomeradditioner. Polymer radical concentration acid during polymerization acid is very small, so termination reactions acid occur only slightly, as these are second order with respect to polymer radical concentration. The technique is experimentally simple and can be carried acid out under bulk conditions or in solution. It usually demands only that the polymerization is carried out under oxygen-free conditions. ATRP has been successfully acid applied to a wide variety of vinyl monomers, for example, substituted styrenes, acrylates and methacrylates, acrylonitrile, (meth) acrylamides acid and (meth) acrylic acids.
Polymers with complex structures acid and built-in functionality A major advantage of ATRP is also that the chain ends of the activity is retained when the polymerization is stopped and the polymer was isolated. Block copolymers are prepared by using the isolated polymer acid as an initiator, so-called macroinitiator acid for the polymerization of a new monomer. This can be repeated and linear block copolymers with many blocks acid or block copolymers with long regular side chains, popularly referred to as polymer brushes are made. Also very regular star-shaped or super branched polymers can be synthesized. Functionalized colloids, surface treated fibers and modified surfaces are produced acid by simultaneously initiate polymerization of multiple, activated sites on the respective objects. As monomers with very different structure, functionality and affinity for example. water can sampolymeriseres this way, the design of a variety of new polymer materials with very specific uses, inter alia, for medical use notice. Specific chemical or physical functionality can be built through special acid monomers or initiator that starts the growing acid polymer chain. Since a large number of different functional groups, for example. of the initiator (e.g., allyl, hydroxy, carboxylic acid, cyano), at the same time has been found not to inhibit the polymerization, acid may be polymers with different chemical end group functionality are prepared. acid Further, the halogen atom at the opposite end of the polymer chain through simple reactions quantitatively transformed to other functional groups, for example. amino, hydroxy, or epoxy. Thus, it is also possible to produce a number of different, very well-controlled linear polymers with different chemical functionality in the two end groups.
Activities of the Danish Polymer Centre Worldwide controlled free-radical polymerization, especially ATRP, now the fastest growing area in polymer chemistry. The Danish Polymer Centre at DTU has controlled acid free-radical polymerization has been a large and active research and education field since its inception in the mid 90s. Two current project concepts acid in design of new polymer materials using ATRP to illustrate the technique scope and potential. Water-soluble polymers with a pH-and concentration-dependent acid morphology Amphiphilic block copolymers containing both hydrophilic (character

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Forget cancer chemotherapy - it's much more effective to spray nano gold rods into the body and heat them up so they toaster cancer cells from the inside. The gold is even no side effect, promising researchers from MIT. By Niels Berg Olsen May 6, 2009 kl. 11:56
The heat is effective as a weapon against cancer cells has long been known, writes Science Daily. The problem has just been that by heating is difficult to avoid damage to healthy tissue adjacent to the tumor.
Geoffrey von Maltzahn says that when treating amide cancer with chemotherapy when 99 percent of the medication did not find cancer cells. But his golden spell that he has received a research award for developing, can bind specifically to cancer cells.
Blood vessels near tumors for the pores, such as nano-rods can penetrate through. The rods are accumulated in the tumor. Radiation in the NIR region (near-infrared) can penetrate the skin cells without damaging them and reach the gold rods, which then heated up to 70 degrees and destroy the cancer cell, they sit in.
Von Maltzahn has developed a polymer coating for gold rods that increases their residence time in the bloodstream significantly. The half-life for their concentration is about 17 hours, which gives them enough time to reach the target. Any excess gold rods flush just out in the urine after a few days the liver and spleen, he said. Documentation
Follow comments
It sounds like it is a completely new and unexplored territory it here. The Texan (Uni of Rice) researcher - Naomi Halas - have worked in the field for some years. She uses simply Gold nano-shells instead of gold rods. Others amide have worked with carbon nanotubes as similar acts as IR absorbing. The (important) work that remains is to get directed nano-particles into the tumor in sufficient concentration.
"SERS-Coded Gold Nanorods as a Multifunctional Platform for densely Multiplexed Near-Infrared Imaging and Photothermal Heating" in the journal. Advanced Materials, Vol.21, p.1-6, 2009; DOI: 10.1002/adma.200803464
The researchers write (with PEG stands for polyethylene glycol rods are covered with and NR stands for nanorod = nano wand): Based on empirical studies of passive tumor targeting, the enhancement of the PEG-NR circulation hour over reported PEG-nanoshell formulations ska amplify sina passive tumor accumulation in tumors, der, in concert with sin enhanced photothermal heat generation in vitro, would forventes amide Provider overall enhanced photothermal contrast mellan tumor and normal tissue.
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Saturday, May 3, 2014

Are we agreed? When they are in a biofilm, maintains the actual social network by communicating cel

Bear rubs
Emil and Esther and Emma are not the only ones small frolicking on the institution's toys. This makes the bacteria and viruses as well. Three healthy scientists now gives bacteria and viruses fight. Read the original article here
Sick with snot and "11-ones" in our children, we soon had enough of. - How many days in winter were you home from work with a snotty kid? - How many of your own sick days could perhaps be traced back to a teddy bear or princess castle web of science in your child's body? - How many sick days have staff mon had - because of the teddy bear? - What is it perhaps cost the whole society, to a teddy bear or other toy spreads "11 metals" to children, parents and staff. Since 2010, the Danish research project "Health in Children's institutions" or SiB, tried to make it clear how to reduce the number of sick days due to "normal" infectious diseases. SiB project has three PhD students (box), each of which examines one of the fundamental aspects of infection at day care: 1 Institution infectious micro organisms. 2 The microbial "community" on surfaces. 3 The potential for active anti-microbial surfaces.
Post-graduate studies in SiB project Explored topic PhD student Bacteria and viruses in day care: identification and occurrence in the environment Tobias Ibfelt doctor Infektionshygienisk Unit Rigshospitalet, University of Copenhagen Coexistence of bacteria in biofilms Genetic characteristics of adhesion to surfaces Jonas Stone Loop Madsen cand. Sc., Biology Department of Biology, University of Copenhagen Nano Fibres for antimicrobial surfaces: Reducing the risk of infection in day care centers Troels HB Eriksen cand. Eng., nanobiotechnology Danish Building Research Insitut, Aalborg University
Day-care institution's second smallest inhabitants - bacteria Which microorganisms "having fun" really with the kids in the toy? Tobias Ibfelt found that there are many bacteria, both respiratory bacteria and intestinal bacteria everywhere in the 23 institutions he studied in Copenhagen, Nyborg and Hørsholm. But most important is that none of these bacteria were pathogenic (ie disease-causing). In contrast, their mere presence on the tables, the bathroom, the kitchen and the toy that in institutions spread content of both snot noses and diapers.
Day-care institution smallest residents - virus Tobias also searched if necessary. web of science pathogenic viruses in the same places in the 23 institutions where he found bacteria. Viruses are not alive but true parasites who always need a living host (as a person, another animal, plant, bacterial, etc.) to multiply in. Virus genes (DNA and RNA), however, can be traced - if enough of it. When people have a viral disease that spews we have lots of virus, so "virus hunter" can easily detect them. But on a toy or a dining table there can be very few and far between DNA and RNA molecules. Therefore, molecules must first be propagated using the PCR method (polymerase chain reaction) web of science before web of science you can track them. Together with DTU Food Tobias had to develop a new method to detect viral genetic material of toys and surfaces. It was found in the tested day care centers, in contrast to the harmless bacteria contained as much as 97% of all samples of different pathogenic viruses. They could include tracked on tables, pillows, nursing pillows, and especially on toys. Most of the samples showed common cold virus (eg. Boca-, rhino-and adenovirus). On the other hand, there was hardly any diarrhea virus (eg. Norovirus and rotavirus, see figure).
Bacteria networks also how the bacteria at the micro level "having fun" at day care, examines Jonas Stone Loop Madsen. Jonas knows that bacteria work best when they are together. They are clearly part literally social networks. Some call it slim - microbiologists call it biofilm, see Fig. We now know that it is actually the bacteria's natural state to exist in a micro-society web of science of interactions, some positive, some negative. Many of the individual bacterial species in the community separator namely polymers, which we see as mucus. Slimy makes both the bacteria adhere better to the surface - such as teddy bears - and that they are resistant to external influences such as drying, chemicals and especially against disinfection.
Are we agreed? When they are in a biofilm, maintains the actual social network by communicating cell and cell from. Here separates each cell a little bit of certain chemical compounds. When the cells as "brands" that the concentration of the compound in their environment is high enough and therefore "marks" that they agree that it is time to change your lifestyle (ie, quorum sensing) to change the behavior. It may be that the metabolism switched to other pathways. Jonas ha

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The keel - from impregnation freeze promotional products drying in shape to Current Conservation
After we had made the reconstruction of the hull form, we know the shape of the keel and work to dry it can get started. The keel is in 8 parts and components have been for impregnating an aqueous solution of PEG 2000 since we received them on the Conservation Department in Brede in 1999. PEG - polyethylene glycol - is a water-soluble, synthetic preservative system promotional products that is reminiscent of wax. It is produced by several different molecular sizes - PEG of high molecular weight is solid at room temperature and not very sensitive to varying humidity. Conversely, PEG having small molecular weight (e.g., 200) completely liquid at room temperature and very hygroscopic. We use PEG 2000 which is solid at room temperature - it is still easy to dissolve in water and it trenger relatively well into the degraded archaeological wood. PEG has the task of replacing any of the material which has disappeared from the old tree in the period it has been in the ground and become degraded. promotional products It takes a long time to impregnate the wood - from 3 to 10 years, depending on how thick the wood is and how open / degraded structure. Keels have been for almost 9 years and have reached the final concentration of 40% PEG 2000.
Ever since we got the goals for the correct shape of the keel, Lotte, our blacksmith, was started making structures that can maintain promotional products keels in the drying process. promotional products Although the tree is broken, we can risikire the work or settle in the drying process. In addition, we must ensure that the keel get the small curvature as reconstruction work has shown that it has had. It requires a solid setup - in order to provide and maintain the tree in the right shape, but also to avoid distortions during the drying process. At the same time our clamps not leave marks in the wood surface or shade for energy transfer in the drying process. It requires good tilrættelægning - not least because we have to work relatively short time with each piece. Once we have taken a køldel by impregnating liquid, the court quickly into place in its support, tightened up and all loose fragments must be put in place. It is very important that the tree does not start to dry while we design and spanning tree up so we pour regularly PEG and water over - and packages keel portions in plastic as soon as we can get to.
When everything is as it should, lifting keel up on a sled and tighten. When all 8 parts are clamped to the sled and wrapped in plastic, push this into the big freeze drying plant. The temperature is set to - 30 C. We have stung temperature sensors into the wood, these are connected to a data logger so we can see when it's all frozen in and quite stiff. So we draw the sled out, take the plastic of pushes the tree into the tank again and close the door securely. Now it takes about 5 months to again we must get hold of the tree - it is the time it takes to freeze dry keel portions .... All køldele wrapped in plastic promotional products before freezing A look through the window into the keels of freeze drying plant. it is not to see, but the temperature is -25 degrees Celsius and the pressure promotional products is o, 1 mbar - ie full vacuum.
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Friday, May 2, 2014

Aricept 5 and 10 mg film-coated tablets contain the active substance is donepezil hydrochloride 5


The content of the leaflets of this website is informative and does not replace the original prospectus (which is included ccdc in the product box). If you have questions, contact your doctor or pharmacist.
Aricept 5 and 10 mg film-coated tablets contain the active substance is donepezil hydrochloride 5 How to store Aricept Store Aricept out of reach of children. Do not store Aricept at temperatures above 30 C. Do not use Aricept after the expiry date stated on the pack. The expiration date is the last day of that month. Only dispose of medicines no longer required at the pharmacy. For environmental reasons, you should not throw medicine in waste water or household waste. 6 Additional ccdc Information ccdc 4.56 mg or 9.12 mg donepezil). ccdc The other ingredients are lactose monohydrate, maize starch, microcrystalline cellulose, hydroxypropyl cellulose, magnesium - stearate, talc, polyethylene glycol, hypromellose and titanium dioxide (E 171). It also contains 10 mg tablets also yellow iron oxide (E172). Appearance and contents of Aricept Appearance Aricept 5 mg is a round, white film-coated tablet marked "5" and "Aricept". Aricept 10 mg is a round, yellow film-coated tablet marked "10" and "Aricept". Pack sizes Aricept 28 and 98 pcs. Aricept 28 and 98 pcs. Not all pack sizes may be marketed. Marketing Authorisation ccdc Holder and Manufacturer Marketing Authorisation Holder PharmaCoDane Ltd. Marielundvej 46 A DK-2730 Herlev Repackaged ccdc and released by PharmaCoDane Ltd. Marielundvej 46 A DK-2730 Herlev read this leaflet carefully before you start taking this medicine Keep this leaflet. You may need to read it again. Ask your doctor ccdc or pharmacist if there is more you want to know. This medicine has been prescribed Aricept for you. You should not give Aricept to others. It may harm them, even if they have the same symptoms you have. Talk to your doctor or pharmacist if any of the side effects gets serious, or notice ccdc any side effects not listed here. Leaflet 1 Effect of Aricept and what it is used for 2 to know before you start taking Aricept 3 How to take Aricept 4 Possible side effects 5 How to store Aricept 6 Further information 1 Effect of Aricept is and what it is used for Aricept is an anti-Alzheimer's dementia. ccdc Aricept belongs to a group of medicines called ccdc acetylcholinesterase - inhibitors. It works by inhibiting the activity of a particular ccdc area of the brain that are important for the symptoms of dementia. They need to take Aricept for Alzheimer dementia in mild to medium severe. The doctor may have given you Aricept for something else. Always follow your doctor's instructions. 2 What you need to know before you start taking Aricept Do not take Aricept , If you are allergic to donepezil, other medicines of the same type (piperidine derivatives) or any of the other ingredients. Take special care with Aricept talk to your doctor before taking Aricept ccdc if you have heart rhythm ccdc disorder or other disease of the heart. have or have had stomach ulcers. have or have had asthma or other lung disease. have problems with the circuit. taking medications for pain or arthritis (NSAID type such as ibuprofen or diclofenac). Contact your doctor if you experience cramps or fainting. It may be a sign of - effect of the heart. problems with urination. movement disorders. Note: If you need anesthesia, the pre tell your doctor ccdc that you are taking Aricept . Always specify the means of blood tests and urine sampling is that you are being treated with Aricept ccdc . It may affect the test results. Taking other medicines Please tell your doctor or pharmacist if you are taking or have recently taken. This includes medicines obtained without a prescription, drugs purchased ccdc abroad, herbal, strong vitamins and minerals and supplements. Tell your doctor if you are taking medication for sponge (ketoconazole, itraconazole) infection (erythromycin) ccdc LEAFLET: ccdc INFORMATION FOR THE USER Aricept 5 mg and 10 mg film-coated tablets donepezil ccdc hydrochloride P620006-B 0809 This leaflet was last revised September 2008. Parallel Distributed and repackaged by PharmaCoDane Ltd., Marielundvej 46 A, DK-2730 Herlev. Aricept PIL_180x270_DK: 1 16.09.2008 11:21 Uhr Seite 1 depression (fluoxetine) tuberculosis (rifampicin) epilepsy (phenytoin) epilepsy and facial neuralgia (carbamazepine) Parkinson's disease (muscle relaxant drugs and other substances that block muscle and nerve functions) and medicine, s