Microcapsules were prepared from [Glu(OMe)] m (Sar) n (m Å 21, n Å 19) and [Lys(Z)] m (Sar) n (m Å 27, n Å 15), and were chemically modified to obtain a pHresponsive releasing membranes. One membrane was prepared by partially deprotecting the ester groups of [Glu(OMe)] m (Sar) n . The other membrane
Preparation, structure and release profile of polypeptide microcapsules
✍ Scribed by Tongjit Kidchob; Shunsaku Kimura; Yukio Imanishi
- Book ID
- 113276028
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 602 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0168-3659
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Microencapsulation of clofibrate and dissolution characteristics of clofibrate microcapsules were investigated. Spherical droplets of clofibrate, prepared by a capillary jet method, were encapsulated in gelatin by simple coacervation, using sodium sulfate as the coacervating agent. The microcapsules
## Abstract In this study, polyethersulfone (PES)–alginate microcapsules were prepared for drug‐controlled release, and vitamin B~12~ (VB~12~), rifampicin (RFP), and bovine serum albumin (BSA) were used as model drugs. Different microcapsules were prepared by the variation of the crosslinking degre