Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Pavan kommavarapu"'
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Akademický článek
Preparation and characterization of rilpivirine solid dispersions with the application of enhanced solubility and dissolution rate
Autor: Pavan kommavarapu, Arthanareeswari Maruthapillai, Kamaraj Palanisamy, Manasvi Sunkara
Publikováno v: Beni-Suef University Journal of Basic and Applied Sciences, Vol 4, Iss 1, Pp 71-79 (2015)
Rilpivirine (RPV) is a pharmaceutical drug used for the treatment of HIV infection. The drug is characterized with poor aqueous solubility and dissolution rate leading to low bioavailability of the drug. Hence, there is a need for the improvement of
Externí odkaz: https://doaj.org/article/eb82e562734d447aa5e19697f255ecb9
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2
In Situ Metastable Form: A Route for the Generation of Hydrate and Anhydrous Forms of Ceritinib
Autor: Saladi Venkata Narasayya, Sudarshan Mahapatra, Prakash Muthudoss, Pavan Kommavarapu, Ravi Teja Koya, R. Ravi Chandra Babu, Ramanaiah Chennuru, Peddy Vishweshwar
Publikováno v: Crystal Growth & Design. 17:6341-6352
Ceritinib is an anaplastic lymphoma kinase (ALK) inhibitor used for the treatment of ALK-positive metastatic non-small cell lung cancer (NSCLC). This BCS class IV drug is developed by Novartis and traded under the name Zykadia. To date two forms [For
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::292295abbcc45ec5c490f71e3595c931
https://doi.org/10.1021/acs.cgd.7b01027
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3
Preparation and characterization of Efavirenz nanosuspension with the application of enhanced solubility and dissolution rate
Autor: Arthanareeswari Maruthapillai, Kamaraj Palanisamy, Pavan Kommavarapu
Publikováno v: HIV & AIDS Review. 15:170-176
Aim Intend of the present exertion is to prepare β-cyclodextrin (β-CD) based polymeric nanosuspension (PNS) of Efavirenz (EFV) with enhanced aqueous solubility and dissolution rate as compared to pure drug. Background EFV is a low aqueous soluble m
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::503db53c5a1b29f95fee5fa79d7d0c50
https://doi.org/10.1016/j.hivar.2016.11.007
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4
Preparation, Characterization and Evaluation of Elvitegravir-Loaded Solid Lipid Nanoparticles for Enhanced Solubility and Dissolution Rate
Autor: Kamaraj Palanisamy, Arthanareeswari Maruthapillai, Pavan Kommavarapu
Publikováno v: Tropical Journal of Pharmaceutical Research; Vol 14, No 9 (2015); 1549-1556
Purpose: To enhance the aqueous solubility and dissolution rate of elvitegravir (EVG) by formulating the drug as solid lipid nanoparticles (SLNs) using solvent injection method.Methods: EVG-loaded SLNs were prepared by solvent injection method. Four
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d55995d37cecfc35e811a8581af697b
https://doi.org/10.4314/tjpr.v14i9.2
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5
Identification and quantitative determination of eletriptan hydrobromide polymorphs: Thermal, diffractometric and spectrometric studies
Autor: Kamaraj Palanisamy, Pavan Kommavarapu, Arthanareeswari Maruthapillai
Publikováno v: Journal of Taibah University for Science. 9(4):586-593
The quantitative characterisation of the solid form of drug substances and drug products is gaining importance due to product quality and performance that is based on stringent regulatory guidelines. Therefore, in this study, thermal, X-ray diffracti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2accd93c189f85cdfff73a995e97d2cc
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6
Preparation and characterization of rilpivirine solid dispersions with the application of enhanced solubility and dissolution rate
Autor: Arthanareeswari Maruthapillai, Kamaraj Palanisamy, Manasvi Sunkara, Pavan Kommavarapu
Publikováno v: Beni-Suef University Journal of Basic and Applied Sciences, Vol 4, Iss 1, Pp 71-79 (2015)
Rilpivirine (RPV) is a pharmaceutical drug used for the treatment of HIV infection. The drug is characterized with poor aqueous solubility and dissolution rate leading to low bioavailability of the drug. Hence, there is a need for the improvement of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec32c1b0667d04892d37cb7aa62dfff0
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8
Physical characterization and dissolution performance assessment of Etravirine solid dispersions prepared by spray drying process
Autor: Pavan, Kommavarapu, Arthanareeswari, Maruthapillai, Kamaraj, Palanisamy, Ravi Teja, Koya
Publikováno v: Pakistan journal of pharmaceutical sciences. 29(6)
The aim of the current exertion was to prepare Solid Dispersion of Etravirine by Spray drying technique to enhance aqueous solubility and dissolution rate. Solid dispersions (SD) of Etravirine were prepared using Copovidone and Povidone-Copovidone in
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::eb62d1a918adfd9b6f1c57d9fa0c780a
https://pubmed.ncbi.nlm.nih.gov/28375119
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9
Simultaneous estimation of degree of crystallinity in combination drug product of abacavir, lamivudine and neverapine using X-ray powder diffraction technique
Autor: Ravikiran Allada, Arthanareeswari Maruthapillai, Kamaraj Palanisamy, Pavan Kommavarapu, Praveen Chappa
Publikováno v: Journal of young pharmacists : JYP. 5(4)
Objective: In the present study, simultaneous determination of degree of crystallinity content in abacavir (ABC), lamivudine (3TC) and neverapine (NVP) from there combination drug product using X-ray powder diffraction (XRPD) technique is developed a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c55632b7c071e295a37156e6f4a26b86
https://pubmed.ncbi.nlm.nih.gov/24563590
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