Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Auzal Halim"'
Publikováno v:
Journal of Pharmacy and Bioallied Sciences, Vol 11, Iss 3, Pp 262-267 (2019)
Gliclazide is a second-generation hypoglycemic sulfonylurea, which is useful in the treatment of non-insulin-dependent diabetes mellitus. It has low bioavailability because of its limited water solubility and slow dissolution rate. In this study, sol
Externí odkaz:
https://doaj.org/article/fe866df4d27d448da0bc87fb31cf96d6
Publikováno v:
Kartika: Jurnal Ilmiah Farmasi, Vol 3, Iss 1, Pp 14-19 (2015)
ABSTRAK Fenilbutazon merupakan obat Anti Inflamasi Non Steroid (NSAID) dan diklasifikasikan dalam kelas II dari biopharmaceutic classification systems (BSC) yang memiliki kelarutan rendah permeabilitas tinggi. Pembentukan kompleks inklusi merupakan s
Externí odkaz:
https://doaj.org/article/c3cdd39136434f1c915a90e3340eda71
Publikováno v:
Indonesian Journal of Pharmacy, Vol 21, Iss 1, Pp 32-39 (2010)
Identification of solid state interaction between TMP and SMZ by hot contact method Kofler and crystallization reaction had been carried out. The results of hot contact method Koflershown formation a new crystalline habit as long and thin needle shap
Externí odkaz:
https://doaj.org/article/604228bd34dc49a798be88209203bd66
Publikováno v:
International Journal of Pharmaceutical Sciences and Medicine. 8:1-7
The mucoadhesive drug delivery system is a drug delivery system in which drugs, along with bioadhesive polymers, are designed to contact longer in the mucous membrane of the gastrointestinal tract. This study aims to formulate glimepiride with sodium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::606b156fa32e3c1d74ee68e6931bf0c0
https://doi.org/10.47760/ijpsm.2023.v08i01.001
https://doi.org/10.47760/ijpsm.2023.v08i01.001
Publikováno v:
International Journal of Applied Pharmaceutics. :251-255
Objective: Glibenclamide belongs to the 2nd generation sulfonylurea group as an oral antidiabetic with low solubility in water and high bioavailability in systemic circulation (Biopharmaceutical Classification System class II). This study aimed to in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82a698db1093a6ae333ddf89c088b7d0
https://doi.org/10.22159/ijap.2022v14i6.46041
https://doi.org/10.22159/ijap.2022v14i6.46041
Publikováno v:
Asian Journal of Pharmaceutical Research and Development. 9:41-47
Celecoxib is a non-steroidal anti-inflammatory drug (NSAID) used for the treatment of pain and inflammation. Celecoxib is included in class II in the Biopharmaceutis ClassificationAsystem drug (BCS) which has low solubility and high permeability. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc91fe70cea9b441b18e19c1d18efc3d
https://doi.org/10.22270/ajprd.v9i6.1037
https://doi.org/10.22270/ajprd.v9i6.1037
Publikováno v:
International Journal of Pharmaceutical Sciences and Medicine. 6:42-51
This review aimed to find information about the solubility of the fenofibrate solid dispersion system using PEG 6000. Fenofibrate is an antihyperlipidemic drug that belongs to the Biopharmaceutical Classification System Class II (BCS II) with low sol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0435d0555b4e1a3a900b22fbe806808b
https://doi.org/10.47760/ijpsm.2021.v06i06.005
https://doi.org/10.47760/ijpsm.2021.v06i06.005
Publikováno v:
JOPS (Journal Of Pharmacy and Science). 4:18-26
Nimodipin merupakan salah satu senyawa yang tidak larut dalam air dan termasuk ke dalam Biopharmaceutical Classification System (BCS) kelas II. Sistem dispersi padat adalah campuran yang homogen dari satu atau lebih bahan aktif dalam matriks yang ine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5ad40f2aecbb34f303208d4e41b8ce7
https://doi.org/10.36341/jops.v4i2.1351
https://doi.org/10.36341/jops.v4i2.1351
Autor:
Henni Rosaini, Yoky Elfadri, Indra Makmur, Wahyu Margi Sidoretno, Auzal Halim, Rina Desni Yetti
Publikováno v:
Ecology, Environment and Conservation. 28:83-83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d477cb305029188e8fd8d8fa1b88c489
https://doi.org/10.53550/eec.2022.v28i01s.083
https://doi.org/10.53550/eec.2022.v28i01s.083
Publikováno v:
JSFK (Jurnal Sains Farmasi dan Klinis), Vol 2, Iss 2, Pp 176-182 (2016)
A study on the effectiveness of liposome delivery system of catechin as an antioxidant has been done. Liposome was derived from phosphatidylcholine of egg and cholesterol. The method used to prepared liposome in this research was thin layer hydration
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::72c8cec161a5617ac38e6c8afcca2d0e
http://jsfkonline.org/index.php/jsfk/article/view/85
http://jsfkonline.org/index.php/jsfk/article/view/85