Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Aqeel A. Fatmi"'
Publikováno v:
Pharmaceutical Research. 27:1318-1324
The goal of the study was to isolate and analyze a cetirizine degradation product, formed within a PEG-containing formulation and to elucidate the mechanism of oxidation of cetirizine. Cetirizine, formulated in PEG-containing matrix, was subjected to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0e325e6d415c3a965b2cd13762b9b64
https://doi.org/10.1007/s11095-010-0114-x
https://doi.org/10.1007/s11095-010-0114-x
Autor:
Derek Bush, Chue Hue Yang, Shingai Majuru, Tatyana Dyakonov, Saujanya Gosangari, Aqeel A. Fatmi
Publikováno v:
Journal of Drug Delivery
Journal of Drug Delivery, Vol 2012 (2012)
Journal of Drug Delivery, Vol 2012 (2012)
The objective of this proof-of-concept study was to develop a platform for controlled drug delivery based on silk fibroin (SF) and to explore the feasibility of using SF in oral drug delivery. The SF-containing matrixes were prepared via spray-drying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85dd7566fff5068a5ced7e076c810d16
https://pubmed.ncbi.nlm.nih.gov/22506122
https://pubmed.ncbi.nlm.nih.gov/22506122
Autor:
Aqeel A. Fatmi, Robert H. Pullen
Publikováno v:
Journal of Chromatography B: Biomedical Sciences and Applications. 574:101-107
Fluvoxamine and nortriptyline, the assay internal standard, were extracted from plasma with ethyl acetate, then reacted with dansyl chloride. The derivatives were quantitated by isocratic reversed-phase high-performance liquid chromatography with flu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bca90e72155a29171714f4ecf228678
https://doi.org/10.1016/0378-4347(92)80103-w
https://doi.org/10.1016/0378-4347(92)80103-w
Autor:
Aqeel A. Fatmi, Gregory V. Williams
Publikováno v:
Drug Development and Industrial Pharmacy. 16:779-789
A high performance liquid chr0matOgraphiC method is presented for the simultaneous determination of hydralazine hydrochloride and hydrochlorothiazide in combination dosage forms. ccmpounds are chromatographed on a radialpak cyanopropylsilane cartridg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::003ed0b0d9b1677bd22c7a0efc6a2a83
https://doi.org/10.3109/03639049009114909
https://doi.org/10.3109/03639049009114909
Simultaneous Determination of Acetaminophen and Hydrocodone Bitartrate in Solid Dosage Forms by HPLC
Autor:
Aqeel A. Fatmi, Gregory V. Williams
Publikováno v:
Journal of Liquid Chromatography. 10:2461-2472
A reversed-phase, high performance liquid chromatographic method is developed and validated for the simultaneous determination of acetaminophen and hydrocodone bitartrate in pharmaceutical dosage forms. The method employs a Radialpak Cyanopropylsilan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::431ff66ac8489dc0a2fbc2ed02e497dd
https://doi.org/10.1080/01483918708068927
https://doi.org/10.1080/01483918708068927
Autor:
Julie A. Johnson, Aqeel A. Fatmi
Publikováno v:
Drug Development and Industrial Pharmacy. 14:1429-1438
An in vitro evaluation of various commercial pancreatic enzyme preparations was undertaken to compare three main types of dosage forms, namely uncoated tablets and powder filled capsules, enteric coated tablets and encapsulated enteric coated microsp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70ee7184b883d424cd523552cb16382f
https://doi.org/10.3109/03639048809151941
https://doi.org/10.3109/03639048809151941
Autor:
Gregory V. Williams, Aqeel A. Fatmi
Publikováno v:
Drug Development and Industrial Pharmacy. 15:1365-1373
A rapid, sensitive, stability indicating, reversed phase HPLC method for the quantitation of Metoclopramide and its related compounds is described. The sample is extracted in methanol and injected on a reverse phase CIS column with a mobile phase of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b95f0bbf70b3b616f72a60c230ae5afc
https://doi.org/10.3109/03639048909062751
https://doi.org/10.3109/03639048909062751
Publikováno v:
Drug Development and Industrial Pharmacy. 10:31-43
A fast, accurate, economical, and reproducible HPLC procedure has been developed to quantitate sulfacetamide (I), sulfabenzamide (II), and sulfathiazole (III) in vaginal creams, using sulfapyridine (IV) as internal standard. The method employed u Bon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9f953e3d706f778dd31c0e70494819e
https://doi.org/10.3109/03639048409038290
https://doi.org/10.3109/03639048409038290
Autor:
Gregory V. Williams, Aqeel A. Fatmi
Publikováno v:
Drug Development and Industrial Pharmacy. 13:2811-2821
The validation of a liquid chromatographic procedure for the determination of acetaminophen, butalbital and caffeine in solid dosage forms is described. The dosage content of tablets or capsules is diluted and chromatographed on a Radialpak Cyanoprop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d4c70581f453737b2a16dc8a36ce66c
https://doi.org/10.3109/03639048709022091
https://doi.org/10.3109/03639048709022091
Publikováno v:
Drug Development and Industrial Pharmacy. 14:711-719
The use of sodium lauryl sulfate in water and 0.1N HC1 as dissolution medium for medroxyprogesterone acetate tablets is investigated. The FDA's handbook of drug dissolution standards recommends the use of 0.54% sodium lauryl sulfate in water as disso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::653135296ca2e1914da87db782868d9b
https://doi.org/10.3109/03639048809151895
https://doi.org/10.3109/03639048809151895