Self-aggregates of poly(2-hydroxyethyl aspartamide) copolymers loaded with methotrexate by physical and chemical entrapments

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Amphiphilic copolymers based on poly(2-hydroxyethyl aspartamide) (PHEA) formed self-aggregates for the entrapment and release of methotrexate (MTX) by physical entrapment and chemical conjugation. In physical entrapment. MTX was partitioned into hydrophobic domains, in self-aggregates of PHEA grafted with octudecyl chains (PHEA-C-18) and the amount of the entrapped drug increased linearly by 3.39 rug per the degree of substitution of grafted octadecyl groups. The amphiphilic nature of the drug induced a large initial release in the buffer medium, irrespective of the amount of octadecyl chains, However, PEG-grafted PHEA-C-18 copolymers conjugated with MTX. ConG, formed a micelle-like structure by self-association of the conjugates and suppressed the initial large release. The alkyl grafting lowered the CAC meaning enhancement of aqueous stability. The release was accelerated in pH 10.0 by rapid hydrolysis of ester linkage by base-catalyzed cleavage, while it was significantly reduced at pH 5.0. (C) 2002 Elsevier Science BM All rights reserved.
Publisher
ELSEVIER SCIENCE BV
Issue Date
2002-05
Language
English
Article Type
Article
Keywords

ACID) BLOCK-COPOLYMER; POLY(ASPARTIC ACID); POLY(GAMMA-BENZYL L-GLUTAMATE); POLY(ETHYLENE OXIDE); LIGHT-SCATTERING; DRUG-RELEASE; DELIVERY; MICELLES; TUMOR; CONJUGATION

Citation

JOURNAL OF CONTROLLED RELEASE, v.81, no.1-2, pp.135 - 144

ISSN
0168-3659
URI
http://hdl.handle.net/10203/83693
Appears in Collection
CBE-Journal Papers(저널논문)
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