Gotowe bibliografie tematyczne / Stability indicating assay

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Gotowa bibliografia na temat „Stability indicating assay”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "Stability indicating assay"

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Thoppil, Simmy O., and P. D. Amin. "Trimetazidine: stability indicating RPLC assay method." Journal of Pharmaceutical and Biomedical Analysis 25, no. 2 (2001): 191–95. http://dx.doi.org/10.1016/s0731-7085(00)00483-0.

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Rajadhyaksha, Namita S., Satish P. Jain, and Purnima D. Amin. "Carbamazepine: Stability Indicating HPLC Assay Method." Analytical Letters 40, no. 13 (2007): 2506–14. http://dx.doi.org/10.1080/00032710701583557.

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Al-Masri, R., and M. Al-Mardini. "STABILITY-INDICATING HPLC ASSAY METHOD OF LOVASTATIN." Bulletin of Pharmaceutical Sciences. Assiut 28, no. 2 (2005): 185–89. http://dx.doi.org/10.21608/bfsa.2005.65287.

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Jamshidi, Ahmad, Hamid Mobedi, and Farzaneh Ahmad-Khanbeigi. "Stability-indicating HPTLC assay for leuprolide acetate." Journal of Planar Chromatography – Modern TLC 19, no. 109 (2006): 223–27. http://dx.doi.org/10.1556/jpc.19.2006.3.10.

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Marwaha, Raj K., Brian F. Johnson, and George E. Wright. "Simple stability-indicating assay for histamine solutions." American Journal of Health-System Pharmacy 42, no. 7 (1985): 1568–71. http://dx.doi.org/10.1093/ajhp/42.7.1568.

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Alam, Prawez, Faiyaz Shakeel, Mohammed H. Alqarni, et al. "Development and Validation of A Stability-Indicating Greener HPTLC Method for the Estimation of Flufenamic Acid." Separations 10, no. 1 (2023): 39. http://dx.doi.org/10.3390/separations10010039.

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The literature on ecofriendly/greener high-performance thin-layer chromatographic (HPTLC) methods for quantifying flufenamic acid (FFA) is scant. In order to develop and validate a stability-indicating greener HPTLC densitometry assay for FFA determination in marketed products, this research was conducted. The ecofriendly eluent system was composed of ethanol–water (70:30 v/v). FFA was measured at 290 nm of wavelength. The greenness scale of suggested analytical assay was derived using “Analytical GREENness (AGREE)” methodology. The suggested stability-indicating HPTLC assay was linear for FFA
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Garcia, Cássia V. "Stability-Indicating HPLC Method for Posaconazole Bulk Assay." Scientia Pharmaceutica 80, no. 2 (2012): 317–27. http://dx.doi.org/10.3797/scipharm.1111-11.

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Sangeetha, M., Tirumala ., and Nagamallika . "STABILITY INDICATING RP-LC ASSAY METHOD FOR CARISOPRODOL." International Journal of Current Pharmaceutical Research 9, no. 6 (2017): 79. http://dx.doi.org/10.22159/ijcpr.2017v9i6.23434.

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Objective: A reverse phase stability-indicating HPLC method was developed for the determination of Carisoprodol in pharmaceutical dosage forms. The chromatographic elution was achieved on C18, 250 mm × 4.6 mm, 5-μm particle size column.Methods: The mobile phase contains a mixture of water and acetonitrile in ratio of 60:40 v/v. The flow rate was 1.0 ml min-1 and was detected by Refractive index detector.Results: The method was proven to be linear over a range of 1 to 4 mg/ml with a mean correlation coefficient of 0.99998. The %mean recovery is in the range of 100.55% to 101.11% and %RSD was le
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Stavchansky, S., B. Eghbali, and R. Geary. "Stability Indicating Assay of Lidocaine Hydrochloride in Solution." Analytical Letters 20, no. 5 (1987): 821–27. http://dx.doi.org/10.1080/00032718708062931.

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Saravanan, G., B. M. Rao, M. Ravikumar, M. V. Suryanarayana, N. Someswararao, and P. V. R. Acharyulu. "A Stability-Indicating LC Assay Method for Bicalutamide." Chromatographia 66, no. 3-4 (2007): 219–22. http://dx.doi.org/10.1365/s10337-007-0280-0.

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Rozprawy doktorskie na temat "Stability indicating assay"

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Kirk, Loren Madden, and Stacy D. Brown. "Beyond-Use Date Determination of Buprenorphine Buccal Solution Using a Stability-Indicating High-Performance Liquid Chromatographic Assay." Digital Commons @ East Tennessee State University, 2015. https://dc.etsu.edu/etsu-works/5305.

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Objectives The objectives of this study included developing and validating a stability-indicating high-performance liquid chromatographic (HPLC) method with ultraviolet (UV) detection for the determination of buprenorphine in a buccal solution for veterinary use, and applying that method to determine the stability of a 3 mg/ml buprenorphine preparation in room temperature and refrigerated storage conditions. This preparation, intended for buccal administration in feline patients, plays an important role in pain management in cats. Methods A stability-indicating HPLC method was developed and va
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Mohammadi, A., I. Haririan, I. Rezanour, L. Ghiasi, and Roderick Walker. "A stability-indicating high performance liquid chromatographic assay for the determination of orlistat in capsules." 2006. http://hdl.handle.net/10962/d1006480.

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A stability-indicating HPLC method was developed and validated for the quantitative determination of orlistat in capsule dosage forms. An isocratic separation was achieved using a Perfectsil® target ODS-3, 250 mm × 4.6 mm i.d., 5 µm particle size column with a flow rate of 0.7 ml/min and using a UV detector to monitor the eluate at 210 nm. The mobile phase consisted of methanol:acetonitrile:trifluoroacetic acid (82.5:17.5:0.01, v/v/v). The drug was subjected oxidation, hydrolysis, photolysis and heat to apply stress conditions. Complete separation was achieved for the parent compound and all d
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Smith, E. W., J. M. Haigh, and I. Kanfer. "A stability-indicating hplc assay with on-line clean-up for betamethasone 17-valerate in topical dosage forms." 1985. http://eprints.ru.ac.za/395/1/haigh_HPLC_assay.pdf.

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A stability-indicating high-performance liquid chromatographic method with on-line clean-up has been developed for the analysis of betamethasone 17-valerate in topical dosage forms. A short pre-column containing 10 μm octadecylsilane mounted into the sample loop position of an injection valve was used as the primary clean-up step. The utilization of a diode-array UV detector allowed the quantitative analysis of betamethasone 17-valerate together with its degradation product, betamethasone 21-valerate, as well as the qualitative analysis of these compounds, relevant internal standards and the p
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陳峙瑞. "Ⅰ.Development of Stability-indicating High Performance Liquid Chromatographic Assay Methods of NSAID Drugs--- Tolmetin and Zomepirac II.Photostability study of Tolmetin." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/61997654301686904495.

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碩士<br>台北醫學院<br>藥學研究所<br>90<br>Abstract Tolmetin (TLM) and Zomepirac (Z) are used as photosensitizing nonsteroidal antiinflammatory drugs (NSAIDs). When TLM and Z were irradiated by a Hanovia 200W high pressure mercury lamp in methanol, a total of 8 photoproducts of TLM; TLM-1 to TLM-8 and 4 photoproducts of Z; Z-1 to Z-4 photoproducts were observed, respectively. Using preparative HPLC, photoproducts were isolated and their chemical structures were elucidated by UV、IR、MS、NMR and LC-MS spectroscopies. Next, a rapid, sensitive, and accurate stability-indicating high perfor-
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Mohammadi, A., N. Rezanour, Dogaheh M. Ansari, Bidkorbeh F. Ghorbani, M. Hashem, and Roderick Walker. "A stability-indicating high performance liquid chromatographic (HPLC) assay for the simultaneous determination of atorvastatin and amlodipine in commercial tablets." 2007. http://hdl.handle.net/10962/d1006340.

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A simple, rapid, precise and accurate isocratic reversed-phase stability-indicating HPLC method was developed and validated for the simultaneous determination of atorvastatin (AT) and amlodipine (AM) in commercial tablets. The method has shown adequate separation for AM, AT from their associated main impurities and their degradation products. Separation was achieved on a Perfectsil® Target ODS-3, 5 μm, 250 mm × 4.6 mm i.d. column using a mobile phase consisting of acetonitrile–0.025 M NaH2PO4 buffer (pH 4.5) (55:45, v/v) at a flow rate of 1 ml/min and UV detection at 237 nm. The drugs were sub
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Smith, E. W., and J. M. Haigh. "In vitro diffusion cell design and validation. I. A stability-indicating high-performance liquid chromatographic assay for betamethasone 17-valerate in purified isopropyl myristate receptor phase." 1989. http://hdl.handle.net/10962/d1006595.

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Introduction: The development of a reliable in vitro permeation system necessitates the use of a precise and accurate method of quantifying the amount of permeant partitioning from the membrane into the cell receptor phase. Aqueous donor and receptor chamber fluids have been used in the majority of reported investigations, which makes quantitative permeant analysis relatively facile. Alternatively, radiolabelled diffusants have been used and flux rates monitored by scintillation counting, obviating the need for chromatographic separation of the receptor-phase components. However, this techniqu
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Książki na temat "Stability indicating assay"

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Rp-Hplc Stability Indicating Assay and Simultaneous Estimation Method for the Combination of Glecapravir and Pibrentasvir in Tablet Dosage Form. Independently Published, 2020.

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Części książek na temat "Stability indicating assay"

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D. China Babu, Dr, G. Sai Sri Harsha, G. Venkateswarlu, M. Alagusundaram, Shailendra Singh Narwariya, and SK Aleesha. "STABILITY INDICATING BIO-ANALYTICAL METHOD DEVELOPMENT AND VALIDATION FOR THE QUANTIFICATION OF APALUTAMIDE - APALUTAMIDE D3 BY USING ULTRA PERFORMANCE LIQUID CHROMATOGRAPHY IN HUMAN PLASMA." In Futuristic Trends in Pharmacy & Nursing Volume 3 Book 4. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bipn4p1ch3.

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A simple, convenient, specific,precise and highly conventional stability indicating ultra performance liquid chromatographic diode array method was developed for the quantification of Apalutamide in human plasma. The phenomenex Luna (100x4.6x5µ) column was used for apalutamide separation and mobile phase was composed with 5 mM ammonium fumarate and acetonitrile in the ratio of 15:85 v/v and buffer pH 3.5 was adjusted with glacial acetic acid and detected at 345 nm. The Apalutamide D3 used as internal standard and K2 EDTA used as coagulant.The liquid liquid extraction process used for extractio
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Godela, Ramreddy, Yagnambhatla Rajendra, Kranthi Kumar Pola, Dr Beda Durgaprasad, and Rani Dumpala. "IMPLEMENTATION OF GREEN SOLVENT SYSTEM FOR THE ANALYSIS OF ADAPALENE IN BULK AND TOPICAL GEL FORMULATION BY RP-HPLC." In Futuristic Trends in Pharmacy & Nursing Volume 2 Book 25. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2023. http://dx.doi.org/10.58532/v2bs25p2ch3.

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A simple and rapid stabilityindicating, RP-HPLC method was ascertained to determine adapalene in bulk and gel formulation. Separation was achieved on enable C18 column (150 x 4.6mm; 5μm) under the isocratic mode of elution by using mobile system mixture of green solvents tetrahydrofuran and methanol (30:70 V/V). The flow rate was maintained at 1.0 ml/min with runtime 10min. UV detection was done at 360 nm. The method was found to be linear for series concentration ranges from 20-100µg/ml. The limit of detection and quantification were found to be 3.27and 0.025µg/ml. Results of precision and ac
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Surekha, MKL, CF Sharon, Sindhu Abraham, and K. Shwetha. "Nanoformulated Epigallocatechin Gallate for its Potential Management of Oral Squammous Cell Carcinoma." In Current Trends in Drug Discovery, Development and Delivery (CTD4-2022). Royal Society of Chemistry, 2023. http://dx.doi.org/10.1039/9781837671090-00376.

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Oral cancer is considered the most active cancer in oral cavity. Potentially malignant lesions in the oral epithelium can eventually develop into oral squamous cell carcinoma.Treating these lesions in the early stages could be an approach for early management of oral cancer. Green tea catechin, Epigallocatechin Gallate (EGCG) has been reported to have anti-oxidative, anti-inflammatory, and anti-tumor activities. In the present work, oral gels containing nanosponges of EGCG were prepared. Nanosponges were formulated using different concentrations of PVA and evaluated for percentage yield, drug
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Sakinala, Padmavathi, Harini Vahika, Ramu Bhadrama raju, Yeellanki Krishnaveni, K. Santhosh, and Sandeep Attinti. "RP-HPLC Method Development and Validation of Stability Indicating Assay for Simultaneous Determination of Pantoprazole, Diclofenac, Chlorzoxazone in Pharmaceutical Dosage Form." In Pharmaceutical Science: New Insights and Developments Vol. 1. BP International, 2024. https://doi.org/10.9734/bpi/psnid/v1/3081.

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Hong, Donald, and Mumtaz Shah. "Development and Validation of HPLC Stability-Indicating Assays." In Drugs and the Pharmaceutical Sciences. CRC Press, 2000. http://dx.doi.org/10.1201/b14011-12.

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Streszczenia konferencji na temat "Stability indicating assay"

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Okocha, Cyril, Tao Chen, Alex Thornton, and Qiwei Wang. "Development of a Squeezable Iron Sulfide Scale Inhibitor for Ultra-Tight Sandstone." In CONFERENCE 2022. AMPP, 2022. https://doi.org/10.5006/c2022-17896.

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Abstract Iron sulfide scaling can manifest both downhole and topside in sour production scenarios. Topsides development can be mitigated via continuous strategic application of an appropriate sulfide scale inhibitor package, however downhole sulfide scaling presents a more complex challenge. Continuous downhole application of sulfide scale inhibitors via capillary string and valve, or routed to valve via existing gas lift architecture are two common delivery options available to the operator, but are unfortunately both limited to providing scale control at injection valve depth and up-string.
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Ferres, H., M. J. Hibbs, and R. A. G. Smith. "THE DEACYLATION OF P-ANISOYL PLASMINOGEN-STREPTOKINASE ACTIVATOR COMPLEX (APSAC, EMINASE™)." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642994.

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The deacylation of the thrombolytic acyl-enzyme APSAC (BRL 26921) has been studied in various media using a radiochemical method. In a buffer containing glycerol, the half-life for deacylation at pH 7.4, 37°C vi/as c. 20-50 min. depending on the concentration of APSAC. The concentration-dependence u/as found to be linked to the availability of free enzyme active centres during the deacylation process and could be normalised to about 50 min. by addition of inhibitors of plasmin or streptokinase, plasmin. In glycerol-free buffer, the deacylation half-life was 147 ± 5 min., indicating that glycer
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Alhajeri, Mubarak Muhammad, Jenn-Tai Liang, and Reza Barati Ghahfarokhi. "Polyelectrolyte Multilayered Nanoparticles as Nanocontainers for Enzyme Breakers During Hydraulic Fracturing Process." In SPE Annual Technical Conference and Exhibition. SPE, 2021. http://dx.doi.org/10.2118/205981-ms.

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Abstract In this study, Layer-by-Layer (LbL) assembled polyelectrolyte multilayered nanoparticles were developed as a technique for targeted and controlled release of enzyme breakers. Polyelectrolyte multilayers (PEMs) were assembled by means of alternate electrostatic adsorption of polyanions and polycations using colloidal structure of polyelectrolyte complexes (PECs) as LbL building blocks. High enzyme concentrations were introduced into polyethyleneimine (PEI), a positively charged polyelectrolyte solution, to form an electrostatic PECs with dextran sulfate (DS), a negatively charged polye
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Raporty organizacyjne na temat "Stability indicating assay"

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Scobie, Linda, Liam O'Connor, Martin D’Agostino, et al. Thermal Inactivation Model for Hepatitis E Virus (HEV). Food Standards Agency, 2022. http://dx.doi.org/10.46756/sci.fsa.sdt366.

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Hepatitis E is an emerging issue, with the number of confirmed cases in the UK increasing in 2009-2015, and decreasing slightly in 2016 and 2017. There is some epidemiological evidence of an association of this virus with undercooked pork and pork products. Currently, there is no standardized method for evaluating thermal stability of HEV and also a lack of a suitable assay that can distinguish between intact HEV that can cause an infection and damaged virus which is not capable of causing an infection. This has raised concerns as it is extremely difficult to extrapolate the risk from pork pro
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Altstein, Miriam, and Ronald J. Nachman. Rational Design of Insect Control Agent Prototypes Based on Pyrokinin/PBAN Neuropeptide Antagonists. United States Department of Agriculture, 2013. http://dx.doi.org/10.32747/2013.7593398.bard.

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The general objective of this study was to develop rationally designed mimetic antagonists (and agonists) of the PK/PBAN Np class with enhanced bio-stability and bioavailability as prototypes for effective and environmentally friendly pest insect management agents. The PK/PBAN family is a multifunctional group of Nps that mediates key functions in insects (sex pheromone biosynthesis, cuticular melanization, myotropic activity, diapause and pupal development) and is, therefore, of high scientific and applied interest. The objectives of the current study were: (i) to identify an antagonist bioph
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