Drug delivery systems based on poly(-caprolactone) for cancer treatment

Autores/as

  • E Sáez-Fernández Departamento de Farmacia y Tecnología Farmacéutica. Facultad de Farmacia. Universidad de Granada, 18071 Granada (Granada). España.
  • MA RUIZ Departamento de Farmacia y Tecnología Farmacéutica. Facultad de Farmacia. Universidad de Granada, 18071 Granada (Granada). España.
  • JL ARIAS Departamento de Farmacia y Tecnología Farmacéutica. Facultad de Farmacia. Universidad de Granada, 18071 Granada (Granada). España.

Palabras clave:

Anti-tumor Drug, Cancer, Controlled Release, Drug Carriers, Drug Delivery, Polymeric Particles, Poly(ε-caprolactone)

Resumen

Chemotherapy agents have little or no specificity over cancer cells, resulting in low therapeutic concentrations at the tumor site (a consequence of a broad systemic distribution), and severe side effects. With the aim of avoiding cancer therapy failure, several approaches such as design of new anticancer drugs, chemical engineering of conventional drugs and development of drug delivery systems have been proposed. The objective is to enhance drug localization at the tumor region (by controlling its biodistribution profile) and, therefore, to increase the anti-tumor efficacy (even in multi-drug resistant tumors), while reducing systemic side effects. One of the most promising approaches to the problem is the development of drug nanocarriers based on the polymer poly(e-caprolactone). In this review we will focus our attention on these polymeric colloids, particularly on the most significant characteristics and formulation procedures, and on their use as nanoplatforms for the delivery of chemotherapy agents to the tumor site. Furthermore, the most recent in vitro and in vivo investigations on the subject are extensively reviewed.

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Publicado

2009-06-20

Cómo citar

1.
Sáez-Fernández E, RUIZ M, ARIAS J. Drug delivery systems based on poly(-caprolactone) for cancer treatment. Ars Pharm [Internet]. 20 de junio de 2009 [citado 22 de diciembre de 2024];50(2):83-96. Disponible en: https://revistaseug.ugr.es/index.php/ars/article/view/5748

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