Enhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation

Puiyan Lee1, Ruizhong Zhang1, Vincent Li1, Xuelai Liu1, Raymond WY Sun2, Chi-Ming Che2, Kenneth KY Wong11Department of Surgery, Li Ka Shing Faculty of Medicine, 2Department of Chemistry and Open Laboratory of Chemical Biology of the Institute of Molecular Technology for Drug Discovery and Synthesis,...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Lee P, Zhang R, Li V, Liu X, Sun RWY, Che CM, Wong KKY
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://doaj.org/article/d657e2769eae463db493c73c63cc4a9d
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:d657e2769eae463db493c73c63cc4a9d
record_format dspace
spelling oai:doaj.org-article:d657e2769eae463db493c73c63cc4a9d2021-12-02T07:14:18ZEnhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation1176-91141178-2013https://doaj.org/article/d657e2769eae463db493c73c63cc4a9d2012-02-01T00:00:00Zhttp://www.dovepress.com/enhancement-of-anticancer-efficacy-using-modified-lipophilic-nanoparti-a9241https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Puiyan Lee1, Ruizhong Zhang1, Vincent Li1, Xuelai Liu1, Raymond WY Sun2, Chi-Ming Che2, Kenneth KY Wong11Department of Surgery, Li Ka Shing Faculty of Medicine, 2Department of Chemistry and Open Laboratory of Chemical Biology of the Institute of Molecular Technology for Drug Discovery and Synthesis, The University of Hong Kong, Hong KongBackground: Development of anticancer drugs is challenging. Indeed, much research effort has been spent in the development of new drugs to improve clinical outcomes with minimal toxicity. We have previously reported that a formulation of lipid gold porphyrin nanoparticles reduced systemic drug toxicity when compared with free gold porphyrin. In this study, we investigated the delivery and treatment efficiency of PEG surface-modified lipid nanoparticles as a carrier platform.Methods: We encapsulated antitumor drugs into PEG-modified lipid nanoparticles and these were characterized by size, zeta potential, and encapsulation efficiency. The delivery efficiency into tumor tissue was evaluated using a biodistribution study. To evaluate antitumor efficacy, gold porphyrin or camptothecin (a DNA topoisomerase I inhibitor) were encapsulated and compared using an in vivo neuroblastoma (N2A) model.Results: We showed that drug encapsulation into PEG-modified lipid nanoparticles enhanced the preferential uptake in tumor tissue. Furthermore, higher tumor killing efficiency was observed in response to treatment with PEG-modified lipid nanoparticles encapsulating gold porphyrin or camptothecin when compared with free gold porphyrin or free camptothecin. The in vivo antitumor effect was further confirmed by study of tumor inhibition and positive apoptosis activity. Surface modification of lipophilic nanoparticles with PEG increased the efficiency of drug delivery into tumor tissue and subsequently more effective antitumor activity.Conclusion: This specific design of a chemotherapeutic agent using nanotechnology is important in the development of a safe and effective drug in cancer therapy.Keywords: lipid nanoparticles, gold porphyrin, cancer, neuroblastoma, camptothecinLee PZhang RLi VLiu XSun RWYChe CMWong KKYDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2012, Iss default, Pp 731-737 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Lee P
Zhang R
Li V
Liu X
Sun RWY
Che CM
Wong KKY
Enhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation
description Puiyan Lee1, Ruizhong Zhang1, Vincent Li1, Xuelai Liu1, Raymond WY Sun2, Chi-Ming Che2, Kenneth KY Wong11Department of Surgery, Li Ka Shing Faculty of Medicine, 2Department of Chemistry and Open Laboratory of Chemical Biology of the Institute of Molecular Technology for Drug Discovery and Synthesis, The University of Hong Kong, Hong KongBackground: Development of anticancer drugs is challenging. Indeed, much research effort has been spent in the development of new drugs to improve clinical outcomes with minimal toxicity. We have previously reported that a formulation of lipid gold porphyrin nanoparticles reduced systemic drug toxicity when compared with free gold porphyrin. In this study, we investigated the delivery and treatment efficiency of PEG surface-modified lipid nanoparticles as a carrier platform.Methods: We encapsulated antitumor drugs into PEG-modified lipid nanoparticles and these were characterized by size, zeta potential, and encapsulation efficiency. The delivery efficiency into tumor tissue was evaluated using a biodistribution study. To evaluate antitumor efficacy, gold porphyrin or camptothecin (a DNA topoisomerase I inhibitor) were encapsulated and compared using an in vivo neuroblastoma (N2A) model.Results: We showed that drug encapsulation into PEG-modified lipid nanoparticles enhanced the preferential uptake in tumor tissue. Furthermore, higher tumor killing efficiency was observed in response to treatment with PEG-modified lipid nanoparticles encapsulating gold porphyrin or camptothecin when compared with free gold porphyrin or free camptothecin. The in vivo antitumor effect was further confirmed by study of tumor inhibition and positive apoptosis activity. Surface modification of lipophilic nanoparticles with PEG increased the efficiency of drug delivery into tumor tissue and subsequently more effective antitumor activity.Conclusion: This specific design of a chemotherapeutic agent using nanotechnology is important in the development of a safe and effective drug in cancer therapy.Keywords: lipid nanoparticles, gold porphyrin, cancer, neuroblastoma, camptothecin
format article
author Lee P
Zhang R
Li V
Liu X
Sun RWY
Che CM
Wong KKY
author_facet Lee P
Zhang R
Li V
Liu X
Sun RWY
Che CM
Wong KKY
author_sort Lee P
title Enhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation
title_short Enhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation
title_full Enhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation
title_fullStr Enhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation
title_full_unstemmed Enhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation
title_sort enhancement of anticancer efficacy using modified lipophilic nanoparticle drug encapsulation
publisher Dove Medical Press
publishDate 2012
url https://doaj.org/article/d657e2769eae463db493c73c63cc4a9d
work_keys_str_mv AT leep enhancementofanticancerefficacyusingmodifiedlipophilicnanoparticledrugencapsulation
AT zhangr enhancementofanticancerefficacyusingmodifiedlipophilicnanoparticledrugencapsulation
AT liv enhancementofanticancerefficacyusingmodifiedlipophilicnanoparticledrugencapsulation
AT liux enhancementofanticancerefficacyusingmodifiedlipophilicnanoparticledrugencapsulation
AT sunrwy enhancementofanticancerefficacyusingmodifiedlipophilicnanoparticledrugencapsulation
AT checm enhancementofanticancerefficacyusingmodifiedlipophilicnanoparticledrugencapsulation
AT wongkky enhancementofanticancerefficacyusingmodifiedlipophilicnanoparticledrugencapsulation
_version_ 1718399546861551616