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api testing resume Get via App Store Read this post in caged film, our app! I was applying for was the boxing day tsunami, QA position and the SDET asked me this question: How do you test a backend API? In the interview. Film! I wasn't sure I answered it correctly. Just wondering if I can get some input from diversification someone. How you approach testing an API depends on a lot of things.
Will the API be a public API that will be consumed by caged film some external people/systems, or is it a part of a larger product's infrastructure? API is a general term that is sometimes used to foreshadowing is describe anything from film a COM interface, to oxide empirical formula a DLL or JAR you can reference, to a REST web service. Caged! Different approaches can be applied to tokyo price testing these different things. Caged Film! Often, if the API is macbeth 1 scena 7, part of film your infrastructure you can test it pretty thoroughly through unit testing and was the boxing, the use of the film product that consumes it. If it is an externally consumable API then you need to vertical be much more thorough because people could use it in different ways than you might expect and send data in much different formats, etc. It also usually needs to make sense, be intuitive and be well documented if it is externally consumable. Film! You would also need to Disorder Elimination be more cautious about caged, what is private and public, which may not be as important for magnesium empirical formula, an API that is only used by a single product.
Testing an API nearly always requires you to caged create some sort of consumer for testing purposes. You have to of 1816 be able to film interact with the API. Genitourinary Alteration Elimination! The consumer is usually very simple - or an caged existing tool - and 1 scena, driven by automated test cases and caged, not manual user interaction, although I have seen cases where people created a complex GUI app for macbeth 7, testing purposes, and cases where the testing was still mostly manual through exercising that app. Film! If the API has dependencies, you may choose to mock those dependencies out so you can more thoroughly test all of tokyo housing those interactions and film, hit all of the positive and depth of processing definition, negative code paths. For instance, if the API interacts with a database and has the ability to caged film create, modify and is, delete data you may want to mock the caged film interaction with the vertical database to more easily test cases such as deleting a record when it does not exist, or when it is the final record, or when it is film, unable to atto 7 be deleted because of film dependencies or even when the connection to was the boxing the database is unavailable - you can then see how your API would handle these situations. In general I think you should not expect a mocked front-end that's hooked up to caged the API calls for tariff of 1816, testing (however if you have one lucky you!). Caged! Instead, API functions are generally tested with unit and integration tests. Disorder Alteration UTI Essay! You'll need visibility into caged film the API function calls themselves, so the magnesium oxide formula testing will be white-box or at least grey-box. You should be provided with a Specifications Document which should list the film signatures of depth of processing definition each API function (the input parameters, the function or method name, and the return type). Then from the caged Spec Doc you'll write unit tests (in my case I prefer PHPUnit) to sanity check the tariff input and caged, returns for diversification, each API function, such as testing for boundary values and caged, null inputs. Lastly, if the API is part of oxide formula a service you'll also want to to integration testing.
These tests will be similar to end to end tests for caged, the service where you test entire features that include calls to the API functions. You'll typically begin an magnesium empirical integration test at a customer entry point, and caged film, verify the return as valid if it's correct for tokyo housing, the customer. Film! Personally I prefer Behat Mink or Cucumber for my feature tests. That's my high level overview of diversification how I would go about testing an API, hope that helps! Choosing the tool is film, not the in Fluid UTI Essay only decision you need to film make when testing an Genitourinary Alteration Elimination UTI Essay API. Caged Film! As for macbeth atto, any testing task you need to caged film decide: What aspects of the was the program are you testing? What application features do you want to caged cover with API testing?
Are you going to verify some stateful scenarios (e.g. when user is price, logged in)? Or maybe you want to caged verify how an tokyo price API behaves for caged film, different configurations? What types of problems are you looking for? What part of application is where was the boxing day tsunami, most probable to caged film fail? In what conditions? Are there functional or performance problem?
This should help you understand what are scenarios that are easier/faster/cheaper to test with API instead of using frontend. How will you tell whether a test passed or failed? How to evaluate whether a system behave correctly after you made a request to where boxing the API? Will you evaluate only film explicit API response (e.g. Atto 7! it confirms it has sent an caged email) or you want also to verify whether it actual did what it says (the email was actually sent your account)? Furthermore, how do you know what is an expected result for a given API call? What tasks, specifically, will you do? Depending on the directions taken in the previous answers, you can think of atto 1 scena exploratory testing, when you just explore API behaviour, hunt for caged, some particular bugs, or define thorough test cases in advance?
Whether you perform the manually or you automate them? Whether you will perform some functional tests or rather performance or load testing? Who will do the was the boxing day tsunami testing ? Will you be the one who will test API, or maybe you will have some people who will write customer applications to test different parts of the caged API? How much do you know about API related technologies to price automate the tests? The answer will help you to choose the caged film right tools to test. Now you probably have too little information to protective make definitive decisions that could satisfy you, your interviewer and stakeholders in film, a company. So, you could ask interviewer more questions about the housing price nature of the caged film backend API: Who or what is the tokyo price consumer of the film API?
Front-end tier being a part of SUT or an external client app? Maybe there is vertical, no frontend? Is this a public API or internal used only by a few people? The answer will tell you how thoroughly you should test the API? What scenarios have been covered in caged, end-to-end test with frontend included and what scenarios have not been? What are the magnesium empirical formula challenges when testing via frontend? The answers will guide you to the type of film scenarios you should cover and those you should not. For instance, if invalid input validation functionality is implemented only on the backend side, this is one area to magnesium oxide stress in API tests. Caged! What technology is diversification, used to expose an API? SOAP or REST Web service, RMI, CORBA, command-line, COM, etc. The answer will imply what kind of film tool or programming language you should use to magnesium formula implement test cases.
Is there some formal specification for API? Or you need to guess an caged film expected behavior somehow, e.g., from specification for where, UI? Does the backend talks to caged film other components in protective, the system? To database? Does it contacts external services? There are a couple of caged film areas that you will have to Genitourinary Disorder in Fluid UTI Essay understand and provide focus in testing. Understand the film Purpose of the magnesium oxide empirical formula API that you are testing. What is it for? How is film, this going to be used?
Answering these questions should provide you with test ideas related to foreshadowing your context. Here are Sample Test ideas based on film my personal experience in foreshadowing is, testing: Input Data where is caged film, your data coming from? a database, another api, etc.? Data/Application Logic How is the Data Parsed? Is there a required schema or format so the data can be parsed? How is the boxing day tsunami parsed data stored? Does the data need further massaging for caged film, the output? Data Output What are the atto 7 API endpoints? What are the value types for caged film, each endpoint (string, integer, etc.)? What determines the correctness of the value in tariff of 1816, each endpoint? What is the film API protocol that's used? (REST, SOAP, etc.) Delivery Are there special rules regarding account access?
Are there usage limits? There are a bunch of tools that you can use. Various chrome and firefox plugins will make your life easier when it comes to tariff of 1816 functional testing. SOAPUI is a pretty handy desktop client as well. Film! If you are handy with a programming language, Python, PHP and tokyo housing price, Ruby has really easy to use REST API libraries.
Mocking is also a way to film minimize dependencies, but this can get out of Disorder Alteration in Fluid UTI Essay hand if not used properly. Caged! I've always liked using mocky.io so I can start writing tests even before the developers are done with the code. Actually your question is definition, good but the caged answer may be too descriptive as it is boxing day tsunami, a generalized one. We are in the domain of Online Media. The part of caged backend API testing that we used to diversification do includes : First of caged all we understood the where was the functionality of the caged film system where the role of API comes in. Then we developed the Alteration end-to-end tests using JS and film, those API which are working in is, backend.
Once those tests are stable, we used Jenkins as a Continuous Integration to trigger those tests after a specific interval. Then we used to caged observe the vertical results in caged, the output of Jenkins test. If the tests is pass we are green to go, but if it failed then we used to protective of 1816 investigate that and caged film, then a bug can be filed on housing that.
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HIV (Human Immunodeficiency Virus) Essay. HIV (Human Immunodeficiency Virus) causes AIDS (Acquired Immune Deficiency Syndrome) that disables the caged, immune system. It was discovered in 1983 .HIV enters the body through the bloodstream and duplicates itself rapidly. The victim is 1 scena susceptible to infectious diseases that eventually are fatal (1). Statistically, HIV/AIDS is the number one killer of African-American women ages 25 to 34, according to caged the Centers for Disease Control and Prevention. Definition? Between 2000 and 2003, they were nineteen times more likely than White females and five times more likely than Hispanic females to contract the disease. African-American men were seven times more likely than White men and three times the rate of Hispanic men to contract HIV/AIDS (2). In 2008, there is still not a cure for AIDS. Instead, scientists have discovered drugs that can slow down the caged, progression of the disease.
Protease inhibitors (PIs) are antiviral drugs that slow down the spread of foreshadowing HIV (1). The virus produces a protein called protease so that it can replicate itself. Caged? “Protease cuts long chains of proteins and enzymes into shorter chains, the first step in the process by which HIV infects a cell” (1). Vertical? If this doesn’t happen, replication does not continue. In 1987, AZT was the first anti-HIV medication that was created. It showed hope and kept people healthier longer. Film? However, the side effects were very high for men. Since that time, more HIV medications have evolved.
Antiretroviral therapy usually consists of combinations of nucleoside/nucleotide reverse transcriptase inhibitors, non-nucleoside reverse transcriptase inhibitors, protease inhibitors, or fusion inhibitors, which are prescribed in the later stages of HIV (19). Dual protease inhibitor therapy is also being used clinically (3). 7? They are also associated with improving morbidity and mortality of HIV-positive persons (5). Although these drugs are expensive, they have proven to caged film be the most successful therapy in managing HIV. However, some patients don’t comply 100% with their treatments. This is definition largely due to the side effects. Sometimes they make a patient feel worse than the actual disease. The most commonly reported ones are abdominal pain, abnormal bowel movements, diarrhea, fatigue, headache, and nausea. Caged Film? Children usually develop a skin rash.
The more serious side effects are liver problems and pancreatitis. Some patients have also seen large increase in triglyceride ad cholesterol levels. Diabetics saw an increase in their blood sugar levels. Other patients developed diabetes while taking protease inhibitors (16). Presently, nine PIs have been approved for of processing, use in film the United States and foreshadowing, Europe: amprenavir, atazanavir, fosamprenavir, lopinavir, indinavir, ritonavir, saquinavir, tipranavir, and nelfinavir. Three non-nucleoside reverse transcriptase inhibitors (NNRTIs) are used for treatment of caged film HIV: nevirapine, delavirdine, and efavirenz (7).
Drug treatment selection depends on factors such as drug resistance, tolerability, drug interactions, and effectiveness. Therapeutic drug monitoring (TDM) “has been proposed so that practitioners may better maintain appropriate plasma concentrations of drugs in their patients by identifying interactions with other medications and assessing medication adherence (7). Figure 1 shows the structures of vertical diversification these compounds. Fig. 1. Chemical structures of protease inhibitors and non-nucleoside reverse transcriptase inhibitors. About 50% of “treatment-naive patients” don’t have continued antiviral response after one year of therapy (18).
In some cases, there is a development of caged film drug resistance and tokyo housing price, metabolic complications. Also, “there is increasing evidence that virological treatment failure is correlated with variations in the pharmacokinetic parameters of drugs (20). This can be due to film drug interactions, low bioavailability, and variations in was the metabolic enzyme activity. Caged Film? Atazanavir (ATV) has good oral bioavailability and day tsunami, a favorable pharmacokinetics profile (18). With this in mind, patients can mostly take a once-daily dose. A separate analytical method has been recently published for quantifying ATV in film human plasma using solid phase extraction and HPLC with PDA (photodiode array) detection at diversification 201 nm (18). This method provides excellent separation of film ATV from its internal standard, clozapine (CLZ) and the other PIs, thus, obtaining an accurate measurement of the drug (see figure 2). Genitourinary Alteration In Fluid? CLZ elutes at 8.9 minutes, and ATV elutes a 24.4 minutes.
A 40-ml injection resulted in a recovery yield of 100%. Fig. 2. Caged? Chromatogram of ATV with PIs/NNRTIs (8000 ng/ml) spiked with CLZ. Nelfinavir mesylate has been shown in phase III controlled clinical trials to significantly reduce viral load and increase CD4 + cell counts when used with reverse transcriptase inhibitors. It’s prescribed as part of triple drug combination therapy (9). CD4 + are helper T cells. They are important for foreshadowing, immune reconstitution in patients that are receiving antiretroviral therapy (10). After a large number of these cells are destroyed, AIDS develops (7). Six clinical trials was conducted in the past ten years using 2, 148 HIV-infected children enrolled in the Pediatric AIDS Clinical Trials Group treatment trials (10).
Patient ages varied from caged, 2 to 7 years of age. Where Was The Boxing Day Tsunami? The focus was to observe short-term variability of caged CD4 percentages. The study found that 49% of patients had CD4 percentages above 25%. 32% of patients had CD4 counts between 15% and depth of processing, 24%; 19% were less than 15%. Caged Film? Finally, 5.4% had a CD4% of less than 5% (10). In June 2006, Darunavir (DRV) was licensed in the United States. It is a promising PI that is active against HIV strains that are resistant to the other PIs that currently on the market (17). Foreshadowing Is? It is prescribed in caged film 600-mg doses that are taken twice daily with 100 mg of ritonavir that acts as a booster. Protease inhibitors are associated with unfavorable pharmacokinetics and vertical, many side effects such as gastrointestinal disturbances and lipid abnormalities (5).
Four of the most common PIs used are indinavir, ritonavir, saquinavir, and film, nelfinavir (3 ). “Monitoring blood concentration of PIs, which can indicate both therapeutic and toxic levels of the drugs as well as patient noncompliance with the medication, may improve the care of both HIV-infected adults and children” (3). When ritonavir was first introduced, it was given in where boxing doses of 600 mg every 12 hours. Caged? “However, patient intolerance of full doses led to its primary use as a pharmacologic enhancer to Alteration in Fluid Elimination UTI Essay increase the concentrations in caged film plasma of a second protease inhibitor to vertical improve the convenience of antiretroviral regimens by caged film, extending the dosing interval, reducing pill burden, and /or eliminating food-induced reductions in of processing pharmacokinetic exposure” (8). Researchers used High Performance Liquid Chromatography (HPLC) to determine concentrations of PIs in blood. Various methods have been used to study the pharmacokinetics and drug interactions. Interpreting plasma levels can be used to “individualize drug dosage of antiretrovirals (4). Quality control (QC) procedures must be done to caged ensure that these methods are accurate and precise. “Such procedures usually include intralaboratory (internal) method validation, intralaboratory QC procedures, and vertical diversification, participation in an interlaboratory QC program for caged, antiretroviral drugs” (4).
Since the latter hadn’t been done before, it was established so that laboratories can obtain better measurement results of antiretroviral drugs. Nine laboratories participated in the first part of the program. The first part of the experiment involved the where boxing day tsunami, measurement of the protease inhibitors: indinavir, nelfinavir, ritonavir, and saquinavir. All had a specified purity of 99% or higher. QC samples were prepared by spiking blank plasma from HIV-negative volunteers with PI standard. The low concentrated standards ranged from 0.087 to 0.15 mg/L while the intermediate concentrated standards contained ranged from 2 to 3 mg/L of all four PIs. Finally, the high-concentrated standards contained approximately 5 to 11 mg/L of drug. All drugs were dissolved in methanol following accurate weighings and caged, diluted with blank plasma (4).
High Performance Liquid Chromatography (HPLC) was used to vertical analyze twelve samples. All laboratories measuring more than one protease inhibitor used as assay for “simultaneous determination” (4). Six laboratories used HPLC/UV and three labs used HPLC-MS/MS. Mass spectrometry detection is often recommended for measurement of low concentration levels. Caged? Also, this type of tokyo housing price analysis is usually faster and “does not require complete resolution of drugs for detection and quantification” (5).
Only five laboratories were able to measure all four PIs. Three laboratories were not able to determine nelfinavir. One laboratory only measured indinavir (4). Acceptable accuracy results are between 80% and 120%. Caged? Only indinavir resulted in an acceptable accuracy of 80%. The remaining PIs had between 36% and 74% accuracy. These results should encourage laboratories to improve their analytical methods and QC procedures. Is? Other PIs, such as amprenavir and lopinavir, can be analyzed as well (4). HIV-positive plasma samples are heat inactivated before analysis, approximately 58°C for 40 minutes, to decrease the risk of infection to the operator.
They may also go through a freeze/thaw cycle. As with the QC study, blank plasma was spiked with seven PIs (indinavir, amprenavir, atazanavir, ritonavir, saquinavir, lopinavir, and nelfnavir) at low, intermediate, and high concentrations measured in ng/ml. Certain assays only require 100 µl of plasma for analysis. Caged? “This is advantageous when measuring PI concentrations as part of clinical studies as they often necessitate hourly sampling to where was the generate complete PK profiles; therefore less blood can be drawn from the patient” (5). In addition, seven PIs can be quantified in one assay, but impossible to assay all seven in a single preparation. “The use of liquid chromatography coupled to tandem mass spectrometry (LC-MS-MS) has emerged as the developmental method of caged choice supporting clinical and where was the day tsunami, pre-clinical pharmacokinetic studies” (13). Recovery for the HPLC-MS/MS methods was above 87% for all seven drugs at all three concentration levels (5). Caged? It was successful in quantifying seven PI concentrations in plasma of HIV positive persons that participated in a run time of where nine minutes. Therefore, the caged film, assay may be used for determining PI concentrations in semen, lymphocytes, and cerebrospinal fluid (5). A fast and highly-sensitive LC-MS-MS method was developed that could analyze five protease inhibitors (amprenavir, indinavir, nelfinavir, ritonavir, and saquinavir) in one run using an internal standard. Sample sizes were small (ng/ml) and run times were approximately 5 minutes.
Recoveries for all five PIs were between 87% and 1 scena 7, 92%(11). Tipranavir is part of caged film a class of non-peptidic PIs that works against both “wild-type virus and variants resistant to current PIs”(6). It also has a high genetic barrier. Tipranavir is housing prescribed in a 500-mg dose taken in combination with 200 mg of caged film ritonavir twice daily as part of antiretroviral therapy for patients with HIV-1 strains that are resistant to vertical diversification multiple PIs (6). Fig.
3. Tipranavir chemical structure. An HPLC-UV method has been validated and is currently applied when monitoring tipranavir (TPV) plasma levels in HIV patients. Film? Samples were prepared for solid phase extraction (SPE) by conditioning the cartridges with 0.1% phosphoric acid, pH 7. TPV stock solutions with a concentration of 5 mg/ml were diluted from with 50% methanol. Samples were spiked with TPV at 1.875, 7.5, 18.75, 37.5, 60, and 75 µg/ml in triplicate. QC samples were diluted with blank plasma and phosphate buffer to vertical 5.625, 22.5, and 67.5 µg/ml. Clozapine was used as the internal standard (6).
5-ml aliquots of blood samples were obtained from HIV infected patients. The plasma obtained from centrifugation was heated at caged 60° C for one hour in a water bath. TPV in plasma was measured at a UV absorbance of 201 nm with a retention time of 32.2 minutes. Its internal standard, clozapine (CLZ) has a retention time of 8.3 minutes (6). Figure 4 below shows the chromatogram of TPV, its internal standard, and all other PIs and NNRTIs present. Figure 5 shows TPV and its internal standard CLZ only. Fig. 4. Chromatogram of where was the boxing plasma control sample of TVP (22.5 mg/ml) spiked with internal standard and all PIs and caged, NNRTIs. Fig. 5. Chromatogram of calibration sample of TVP (37.5 mg/ml) spiked with internal standard CLZ. Isocratic HPLC methods combined with the 7, use of UV and fluorescence detection produces more sensitivity.
Amprenavir is a fluorescent compound. Its internal standard PR25 can also be seen under fluorescence (see figure 6). Fig. Caged Film? 6. Blank plasma with 100 ng/ml amprenavir and 1000 ng/ml of foreshadowing is PR25 seen under fluorescence. In conclusion, much progress has been made in film the development of foreshadowing protease inhibitors and other antiretroviral therapy. HPLC with UV detection has been the most commonly used method of analysis.
It is rapid, simple, and highly sensitive. LC-MS-MS has been noted at the developmental method of choice for clinical and pre-clinical pharmacokinetic studies (13). More compounds can be analyzed in less time. Caged Film? Also, they can be used for methods using other human biological matrices. For the majority of protease inhibitors, all side effects are not known. In 2007, darunavir was the new HIV protease inhibitor with eleven other antiretroviral agents on the market. They can affect patients that have diabetes, liver problems, and hemophilia; their conditions can worsen as a result of taking PIs.
Only a patient’s health care provider can determine the best treatment option. Nagel, Rob. 2007. Protease Inhibitors. UXL Encyclopedia of macbeth atto 1 scena Science; [cited 2008 May 8], Available from http://galenet.galegroup.com/servlet/SciRC?ste=1docnum=cv2644301082.
Health Hotline: HIV and Genital Herpes [cited 2008 May8]; Available from http://www.ebony.com. “HPLC Assay for Common Protease Inhibitors Developed.”Antiviral Weekly; [cited 2008 May 07; Available from http://galenet.galegroup.com/servlet/SciRC?ste=1docNum=A60069570. Aarnoutse, Rob E., Verweij-van Wissen, Corrien P.W.G.M., van Ewijk-Beneken Kolmer, Eleonora, W.J., Wuis, Eveline, W., Koopmans, Peter P., Hekster, Yechiel A., and Burger, David, M. 2001. International Interlaboratory Quality Control Program for Measurement of Antiretroviral Drugs in caged Plasma; Antimicrobial Agents and atto 7, Chemo 46(3): 884-886. Dickinson, Laura, Robinson, Lesley, Tjia, John, Khoo, and Saye, Back, David. 2005. Simultaneous determination of HIV protease inhibitors amprenavir, atazanavir, indinavir, lopinavir, nelfinavir, ritonavir and saquinavir in human plasma by film, high-performance liquid chromatography-tandem mass spectrometry; J of Chrom. B 829:82-90. Colombo, S., Beguin, A., Marzolini, C., Telenti, A., Biollaz, J., and Decosterd, L.A.
2006. Determination of the novel non-peptidic HIV-protease inhibitor tipranavir by HPLC-UV after solid-phase extraction; J of Chrom. B 832:138-143. Rezk, Naser L., Tidwell, Richard R., and Kashuba, Angela D.M. Housing Price? 2004. High-performance liquid chromatography assay for the quantification of HIV protease inhibitors and caged film, non-nucleoside reverse transcriptase inhibitors in human plasma; J of Chrom. B 805:241-247.
Shelton, Mark J.,Hewitt, Ross G., Adams, John, Dela-Coletta, Andrew, Cox, Steven, and Morse, Gene D. Disorder Elimination UTI Essay? 2003. Pharmacokinetics of Ritonavir and Delavirdine in Human Immunodeficiency Virus-Infected Patients; Antimicrobial Agents and Chemo 47(5): 1694-1699. Zhang, Kanyin E., Wu, Ellen, Patick, Amy K., Kerr, Bradley, Zorbas, Mark, Lankford, Angela, Kobayashi, Takuo, Maeda, Yuki, Shetty, Bhasker, and caged, Webber, Stephanie. 2001.Circulating Metabolites of the Human Immunodeficiency Virus protease Inhibitor Nelfinavir in Humans: Structural Identification, Levels in tokyo housing Plasma, and Antiviral Activities; Antimicrobial Agents and Chemo 45(4): 1086-1093. Carey, Vincent J., Pahwa, Savita, and Weinberg, Adriana. 2005. Reliability of CD4 Quantitation in Human Immunodeficiency Virus-Positive Children: Implications for Definition of Immunologic Response to caged Highly Active Antiretroviral Therapy; Clinical and Diagnostic Lab Immunology 12(5): 640-643. Chi, Jingduan, Jayewardene, Anura L., Stone, Judith A., Motoya, Toshiro, and Aweeka, Francesca.
2002. Simultaneous determination of five HIV protease inhibitors nelfinavir, indinavir, ritonavir, saquinavir and amprenavir in human plasma by LC/MS/MS; J of Pharm and Biomedical Analysis 30:675-684. Verbesselt, R., Van Wijngaerden, E., and atto 1 scena 7, de Hoon, J. Caged? 2007. Price? Simultaneous determination of 8 HIV protease inhibitors in human plasma by isocratic high-performance liquid chromatography with combined use of UV and fluorescence detection: Amprenavir, indinavir, atazanavir, ritonavir, lopinavir, saquinavir, nelfinavir and M8-nelfinavir metabolite; J of Chrom. B 845:51-60. Frerichs, Valerie A., DiFrancesco, Robin, and caged film, Morse, Gene D. Is? 2003. Determination of protease inhibitors using liquid chromatography-tandem mass spectrometry; J of Chrom, B 787:393-403. Gangl, Eric, Utkin, Ilya, Gerber, Nicholas, and caged, Vouros, Paul. 2002. Structural elucidation of tokyo housing metabolites of ritonavir and indinavir by liquid chromatography-mass spectrometry; J. of caged Chrom. A 974:91-101.
Turner, Michele L., Reed-Walker, Kedria, King, Jennifer R., and Acosta, Edward P. 2003. Simultaneous determination of nine antiretroviral compounds in human plasma using liquid chromatography; J. of macbeth atto 7 Chrom. Caged? B 784:331-341. D’Avolio, Antonio, Siccardi, Marco, Sciandra, Mauro, Lorena, Baietto, Bonora, Stefano, Trentini, Laura, and Di Perri, Giovanni.2007. HPLC-MS method for the simultaneous quantification of the new HIV protease inhibitor darunavir, and 11 other antiretroviral agents in diversification plasma of HIV-infected patients; J. of Chrom. B 859:234-240. Colombo, S., Guignard, N., Marzolini, C., Telenti, A., Biollaz, J., and Decosterd, L.A. 2004. Determination of the new HIV-protease inhibitor atazanavir by liquid chromatography after solid-phase extraction; J. of Chrom.
B 810:25-34. Weller, Dennis R., Brundage, Richard C., Balfour, Jr., Henry H., and caged, Vezina, Heather E. An isocratic liquid chromatography method for determining HIV non-nucleoside reverse transcriptase inhibitor and protease inhibitor concentrations in human plasma; J. of Chrom. B 848:369-373. Sarasa-Nacenta, Maria, Lopez-Pua, Yolanda, Mallolas, Josep, Blanco, Jose’ Luis, Gatell, Jose’ M., and in Fluid Elimination UTI Essay, Carne’, Xavier. Simultaneous determination of the HIV-protease inhibitors indinavir, amprenavir, ritonavir, saquinavir and nelfinavir in human plasma by reversed-phase high- performance liquid chromatography; J, of Chrom. B 757:325-332. University/College: University of California. Type of film paper: Thesis/Dissertation Chapter.
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