Výsledky vyhledávání - "U. V. S. Sara"

Development of a new HPLC method for in vitro and in vivo studies of haloperidol in solid lipid nanoparticles

Autor: U. V. S. Sara, Mohd Yasir, Iti Som

Publikováno v: Brazilian Journal of Pharmaceutical Sciences; Vol. 53 No. 2 (2017); e16047
Brazilian Journal of Pharmaceutical Sciences; Vol. 53 Núm. 2 (2017); e16047
Brazilian Journal of Pharmaceutical Sciences; v. 53 n. 2 (2017); e16047
Brazilian Journal of Pharmaceutical Sciences
Universidade de São Paulo (USP)
instacron:USP
Brazilian Journal of Pharmaceutical Sciences, Volume: 53, Issue: 2, Article number: e16047, Published: 22 JUN 2017
Brazilian Journal of Pharmaceutical Sciences, Vol 53, Iss 2 (2017)

A simple and sensitive HPLC method was developed and validated for the quantification of haloperidol in solid lipid nanoparticles (SLNs). The developed method was used for detection of shelf life of haloperidol in SLNs. Calibration curve of haloperid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93c6d9b2731dcd2e48f174f84a2780de
https://www.revistas.usp.br/bjps/article/view/134168

Zobrazit plný text záznamu

Solid lipid nanoparticles for nose to brain delivery of haloperidol: in vitro drug release and pharmacokinetics evaluation

Autor: Mohd Yasir, U. V. S. Sara

Publikováno v: Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica B, Vol 4, Iss 6, Pp 454-463 (2014)

In the present study, haloperidol (HP)-loaded solid lipid nanoparticles (SLNs) were prepared to enhance the uptake of HP to brain via intranasal (i.n.) delivery. SLNs were prepared by a modified emulsification–diffusion technique and evaluated for

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97906d3d891b2e792b58c23fd3307c27
http://europepmc.org/articles/PMC4629108

Zobrazit plný text záznamu

Preparation and optimization of haloperidol loaded solid lipid nanoparticles by Box–Behnken design

Autor: U. V. S. Sara, Mohd Yasir

Publikováno v: Journal of Pharmacy Research. 7:551-558

Background The aim of this investigation was to design and evaluate solid lipid nanoparticles (SLNs) of haloperidol. Method A modified solvent emulsification diffusion technique was used to produce Haloperidol loaded solid lipid nanoparticles. A 3-fa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4b290827d779fd6359b326d3ac2b025b
https://doi.org/10.1016/j.jopr.2013.05.022

Zobrazit plný text záznamu

Development and Validation of a New HPLC Method for In-vitro Studies of Haloperidol in Solid Lipid Nanoparticles

Autor: U. V. S. Sara, Lubhan Singh, Iti Som, Mohd Yasir

Publikováno v: Journal of Analytical & Bioanalytical Techniques.

A simple and sensitive HPLC method was developed and validated for the study of in-vitro drug release from haloperidol loaded solid lipid nanoparticles (SLNs). The method was also used for the analysis of drug for detection of shelf life of developed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9c8a3cae284d00ca0b9ac40a426b20a5
https://doi.org/10.4172/2155-9872.1000339

Zobrazit plný text záznamu

Design, development, physicochemical, in vitro and in vivo evaluation of monolithic matrix type transdermal patches containing nitrendipine

Autor: Asgar Ali, Aqil Mohammed, U. V. S. Sara, Ashu Mittal

Publikováno v: Pharmaceutical Development and Technology. 14:422-434

The matrix type transdermal drug delivery systems (patches) of Nitrendipine were prepared by film casting technique. The patches were characterized for physical, in vitro release studies and ex-vivo permeation studies (human cadaver skin). On the bas

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::024014a0e6bd53fb2d350dbb24d7b29f
https://doi.org/10.1080/10837450902748388

Zobrazit plný text záznamu

Plný text ve formátu HTML

Synthesis, characterization, and in vitro drug release study of methacrylate diclofenac conjugate as macromolecular prodrug

Autor: Neeraj, Agrawal, M J N, Chandrasekar, U V S, Sara, A, Rohini

Publikováno v: PDA journal of pharmaceutical science and technology. 64(4)

Diclofenac was covalently coupled to 2-hydroxyl ethyl methacrylate (HEMA) to get a monomeric drug derivative of diclofenac. This monomer was subjected to radicular polymerization to get poly(diclo-EMA) conjugate. The in vitro drug release study of th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9399203a1917b3a6a1be40263987624c
https://pubmed.ncbi.nlm.nih.gov/21502035

Zobrazit plný text záznamu

Poly(HEMA-Zidovudine) conjugate: a macromolecular pro-drug for improvement in the biopharmaceutical properties of the drug

Autor: U. V. S. Sara, Agrawal Neeraj, A Rohini, M.J.N. Chandrasekar

Publikováno v: Drug delivery. 18(4)

A macromolecular pro-drug of a known anti-viral agent Zidovudine (AZT) was synthesized and evaluated as a sustained drug delivery system. The pro-drug was synthesized by coupling the drug to 2-hydroxyethyl methacrylate (HEMA) through a succinic space

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::474a19e9f05827e215a2fe08e622807f
https://pubmed.ncbi.nlm.nih.gov/21110710

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání