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Cited by 294

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Preparation of micelle-forming polymer-drug conjugates

Yokoyama, Masayuki, Kwon, Glenn S., Okano, Teruo, Sakurai, Yasuhisa, Seto, Takashi, Kataoka, Kazunori·1992·Bioconjugate Chemistry

Abstract

Adriamycin, a hydrophobic anticancer drug, was conjugated with poly(ethylene oxide)-poly(aspartic acid) block copolymers composed of various lengths of each block copolymer segment ranging from 1000 to 12,000 in molecular weight and from 10 to 80 units, respectively. Conjugation was achieved without precipitation by adjusting the ratio of adriamycin to aspartic acid residues of the block copolymer and the quantity of DMF used for the reaction. Thus obtained conjugates showed high water solubility irrespective of a large amount of the conjugated adriamycin. Furthermore, these conjugates were found to form micellar structures with a hydrophobic inner core and a hydrophilic outer shell. This micellar architecture may be utilized for effective drug targeting.

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Crossref · 10.1021/bc00016a007

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Metadata

Authors
Yokoyama, M., Kwon, G. S., Okano, T., Sakurai, Y., Seto, T., & Kataoka, K.
Venue
Bioconjugate Chemistry
Published
1992-07-01
Volume
3
Issue
4
Pages
295-301
ISSN
  • 1043-1802 (ISSN-L)
  • 1520-4812
OpenAlex
W1999903282
Cited by
294
References
2
FWCI
7.05
Type
journal article
Language
en
Open access
closed

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.