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2000
Volume 16, Issue 10
  • ISSN: 1871-5206
  • E-ISSN: 1875-5992

Abstract

In this paper, we report on a potential cancer drug delivery system that utilizes the ligand targeting of the folate receptor. Our drug delivery system consists of Pluronic-P105 micelles, targeted with folic acid moieties. A melanoma folate positive (FR+) (B16-F10), and a fibroblast folate negative (FR-) (NIH-3T3) cell lines are used to compare the cellular accumulation of a chemotherapeutic drug (Doxorubicin) when the delivery is mediated by folated Pluronic P105 micelles. In order to obtain a proper comparison, we corrected for the quenching of Doxorubicin by folic acid molecules and illustrated the significant effect of quenching on the analysis of similar systems. Results show an 80% increase in the accumulation of the antineoplastic agent in the FR+ cell line, when compared to the FR- cell line, thus providing evidence that the efficacy of Pluronic micelles, as drug delivery vehicles, can be enhanced via folic acid targeting.

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/content/journals/acamc/10.2174/1871520616666160219161600
2016-10-01
2025-04-04
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/content/journals/acamc/10.2174/1871520616666160219161600
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  • Article Type:
    Research Article
Keyword(s): active targeting; B16-F10; Doxorubicin; folate; melanoma; micelles; quenching
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