Preparation of poly(NIPAAm)-Pluronic F68 as a thermosensitive surfactant for a controlled drug release [0.03%]
聚NIPAAm-普朗尼克F68温敏表面活性剂的合成及控释研究
Sung-Wook Choi,Hye Min Lee,Tae-Joon Park et al.
Sung-Wook Choi et al.
This paper describes the synthesis of thermosensitive surfactants by polymerizing N-isopropylacrylamide (NIPAAm) into the Pluronic F68 surfactant and their application for a controlled drug release. Poly(NIPAAm)-Pluronic surfactants with di...
Developing micro-/nanoparticulate drug delivery systems using "design of experiments" [0.03%]
采用“实验设计法”开发微/纳米粒药物递送系统
Bhupinder Singh,Rahul Bhatowa,Chandra Bhushan Tripathi et al.
Bhupinder Singh et al.
Of late, micro and nanoparticluate drug delivery systems have been gaining immense importance primarily attributed to their improved drug release controlling and targeting efficiencies. Also, the small particle size and desirable surface ch...
Ch Saroja,Pk Lakshmi,Shyamala Bhaskaran
Ch Saroja
Vaccines are the preparations given to patients to evoke immune responses leading to the production of antibodies (humoral) or cell-mediated responses that will combat infectious agents or noninfectious conditions such as malignancies. Alar...
Nanopharmaceutics [0.03%]
纳米药学
Javed Ali
Javed Ali
Chemical stability of tramadol hydrochloride injection admixed with selected pain drugs [0.03%]
tramadol氯化氢与几种镇痛药配伍的化学稳定性研究
V Di Stefano,R Pitonzo,S Bavetta et al.
V Di Stefano et al.
Background: Tramadol hydrochloride (HCl) and ketorolac tromethamine are analgesic drugs, which are commonly used in combination in postoperative pain management. According to some studies, metoclopramide and magnesium sul...
Y Indira Muzib,K Srujana Kumari
Y Indira Muzib
Background: Glibenclamide is an oral hypoglycemic drug completely metabolized in the liver, the principal metabolite being very weakly active, buccal delivery may be useful for the treatment of diabetes more effectively. ...
Roonal L Jain,J P Shastri
Roonal L Jain
Background: This project aims to formulate and characterize a drug-eluting contact lens to provide controlled release of drug for a longer period of time, using liposomes as drug delivery system. ...
Dissolution enhancement of efavirenz by solid dispersion and PEGylation techniques [0.03%]
采用固体分散技术和PEG修饰技术改善依非韦伦的溶解度
B Bindu Madhavi,B Kusum,Ch Krishna Chatanya et al.
B Bindu Madhavi et al.
Background: Efavirenz is the preferred nonnucleotide reverse transcriptase inhibitor for first-line antiretroviral treatment in many countries. It is orally active and is specific for human immunodeficiency virus type 1. ...