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Lapachone delivery systems, compositions and uses related thereto

a technology of lapachone and composition, applied in the field of potent cytotoxic agents, can solve the problems of limiting the potential systemic administration and clinical application of lapachone, limiting the solubility of common solvents, and limiting the solubility or bioavailability of lapachone. the effect of improving the solubility or bioavailability of lapachon

Inactive Publication Date: 2005-08-11
CASE WESTERN RESERVE UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention is about a system that includes a lapachone or prodrug thereof and a biocompatible polymer. The system can be used for the treatment of malarial, fungal, parasitic, and viral infections. The polymer can also include other biologically active agents or diagnostic agents. The system can be in the form of microspheres or nanospheres, which can be administered to patients through various methods such as injection or inhalation. The use of the polymer system allows for sustained release of the therapeutic agent and can provide different treatment regimens compared to other methods.

Problems solved by technology

Because cancer cells are constantly replicating and circumvent many mechanisms that restrict replication in normal cells, they are more vulnerable to topoisomerase inhibition than are normal cells.
Despite the potency and selectivity of β-lap in killing cancer cells in vitro, the low water solubility of β-lapachone (0.04 mg / ml or 0.16 mM) limits its potential for systemic administration and clinical applications in vivo. β-lapachone is highly insoluble in water and has only limited solubility in common solvent systems used for topical and parenteral administration.

Method used

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  • Lapachone delivery systems, compositions and uses related thereto
  • Lapachone delivery systems, compositions and uses related thereto
  • Lapachone delivery systems, compositions and uses related thereto

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Embodiment Construction

1. Overview

[0037] The present invention relates to strategies for the delivery of a lapachone or a prodrug thereof to a patient in need thereof, including sustained release delivery, through a wide variety of routes, including microspheres and nanospheres for injection or inhalation. The polymers can be prepared using clinically approved monomers, including lactic acid (LA), glycolic acid (GA), sebacic acid (SA), 1,3-bis(carboxyphenoxy)propane (CPP), and blocks of poly(lactic-co-glycolic acid) (PLGA) and / or poly(ethylene glycol) (PEG) of various molecular weights. By varying their composition, the properties of drug-loaded particles made from these polymers can be optimized. For example, surface properties can be tuned to improve aerosolization efficiency; phagocytic particle clearance in the deep lung can be inhibited by the presence of PEG in the polymer backbone (and ultimately on the particle surface); and continuous drug delivery kinetics can be achieved with control over tot...

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Abstract

In part, the present invention is directed to a system comprising a lapachone or a prodrug thereof and a polymer, such as a biocompatible and optionally biodegradable polymer, methods for treatment using the subject polymer compositions, and methods of making and using the same. In another part, the present invention includes inclusion complexes of a lapachone or a prodrug thereof and a cyclodextrin, preferably a β-cyclodextrin, such as hydroxypropyl β-cyclodextrin, e.g., to improve the solubility of the lapachone or prodrug thereof.

Description

RELATED APPLICATION [0001] This application claims the benefit of, and incorporates by reference, the entire disclsoure of U.S. Provisional Patent Application No. 60 / 374693, filed Apr. 23, 2002.BACKGROUND OF THE INVENTION [0002]β-Lapachone (β-lap) is a potent cytotoxic agent that demonstrates antitumor activity against a variety of human cancer cells at concentrations typically in the range of 1-10 μM (IC50). The drug was first isolated from the bark of the Lapacho tree (genus Tabebuia) in the rainforests of South America, which has a long history as an herbal medicine. Cytotoxicity has been demonstrated in transformed cell lines derived from patients with promyelocytic leukemia, prostate, malignant glioma, hepatoma, colon, breast, ovarian, pancreatic, and multiple myeloma cell lines including drug-resistant lines. (Planchon et al., Cancer Res., 55 (1996) 3706; Li, C. J., et al., Cancer Res., 55 (1995) 3712; Weller, M. et al., Int. J Cancer, 73 (1997) 707; Lai, C. C., et al. Histol ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K9/00A61K31/35A61K31/352A61K31/353A61K31/724A61K47/34A61K47/40A61K47/48A61K51/12
CPCA61K9/0024A61K31/35A61K31/352A61K31/353A61K31/724B82Y5/00A61K47/40A61K47/48969A61K51/1268A61K51/1282A61K47/34A61K47/6951
Inventor BOOTHMAN, DAVIDGAO, JINMINGNASONGKLA, NORASEDPINK, JOHN
Owner CASE WESTERN RESERVE UNIV