Liposomal formulation and antitumor activity of 14-O-palmitoyl-hydroxyrubicin

Roman Perez-Soler, Waldemar Priebe

Research output: Contribution to journalArticle

7 Scopus citations

Abstract

The 14-O-palmitoyl ester of 3′-deamino-3′-hydroxydoxorubicin was synthesized to study the liposomal formulation and biological activity properties conferred by the attachment of a lipophilic group to position 14 of the anthracycline molecule. The entrapment efficiency of 14-O-palmitoyl-hydroxyrubicin in multilamellar vesicles composed of dimyristoylphosphatidyl choline and dimyristoylphosphatidyl glycerol was >99%. In addition, the stability of liposomes containing 14-O-palmitoyl-hydroxyrubicin was >99% at 14 days as assessed by the amount of drug leaking out of the liposomes and the absence of crystals of free drug in the liposome pellet. Esterilication at position 14 did not significantly decrease the potency of the parent compound 3′-hydroxydoxorubicin. Liposome-entrapped 14-O-palmitoyl-hydroxyrubicin was significantly more active than doxorubicin against two murine tumor models. Against ip L-1210 leukemia, liposome-entrapped 14-O-palmitoyl-hydroxyrubicin injected i.p. into mice at doses of 60 and 80 mg/kg resulted in a %T/C value (median survival of treated/control animals ×100) of >600, with 3-4 of 6 animals being cured, where-as in the same experiments, doxorubicin injected at the optimal dose (10 mg/kg) resulted in a %T/C value of 340, with 1 of 6 animals being cured. In animals bearing liver metastases of M-5076 reticulosarcoma, liposome-entrapped 14-O-palmitoyl-hydroxyrubicin showed significant antitumor activity when given on a three-i.v.-injection scheule of 20 mg/kg on days 4, 8, and 12 (%T/C, 175), whereas doxorubicin injected at optimal doses of 6-8 mg/kg on the same days was devoid of antitumor activity (%T/C, 129-133). These results indicate that esterification at position 14 enhances the affinity of this type of compounds for lipid bilayers without negatively affecting their biological activity.

Original languageEnglish (US)
Pages (from-to)267-271
Number of pages5
JournalCancer Chemotherapy and Pharmacology
Volume30
Issue number4
DOIs
Publication statusPublished - Jul 1 1992
Externally publishedYes

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ASJC Scopus subject areas

  • Oncology
  • Toxicology
  • Pharmacology
  • Cancer Research
  • Pharmacology (medical)

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