Nanomedicine review: clinical developments in liposomal applications

Abstract Background In recent years, disease treatment has evolved strategies that require increase in pharmaceutical agent’s efficacy and selectivity while decreasing their toxicity in normal tissues. These requirements have led to the development of nanoscale liposome systems for drug release. Thi...

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Main Authors: Esteban Beltrán-Gracia, Adolfo López-Camacho, Inocencio Higuera-Ciapara, Jesús B Velázquez-Fernández, Alba A Vallejo-Cardona
Format: Article
Language:English
Published: BMC 2019-12-01
Series:Cancer Nanotechnology
Subjects:
Online Access:https://doi.org/10.1186/s12645-019-0055-y
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spelling doaj-e94cb74995ed4cbf8254d419414616192020-12-20T12:17:45ZengBMCCancer Nanotechnology1868-69581868-69662019-12-0110114010.1186/s12645-019-0055-yNanomedicine review: clinical developments in liposomal applicationsEsteban Beltrán-Gracia0Adolfo López-Camacho1Inocencio Higuera-Ciapara2Jesús B Velázquez-Fernández3Alba A Vallejo-Cardona4Departamento de Biotecnología Médica Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ)Departamento de Biotecnología Médica Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ)Departamento de Tecnología Alimentaria, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CIATEJ)Departamento de Tecnología Ambiental, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CONACYT-CIATEJ)Departamento de Biotecnología Médica Farmacéutica, Centro de Investigación y Asistencia en Tecnología y Diseño del Estado de Jalisco (CONACYT-CIATEJ), A. C.Abstract Background In recent years, disease treatment has evolved strategies that require increase in pharmaceutical agent’s efficacy and selectivity while decreasing their toxicity in normal tissues. These requirements have led to the development of nanoscale liposome systems for drug release. This review focuses on lipid features, pharmacological properties of liposomal formulations and the clinical studies of their application. Main body Several lipids are available, but their properties could affect pharmacological or clinical efficiency of drug formulations. Many liposomal formulations have been developed and are currently on the market. Proper selection of lipid is essential for the pharmacological effect to be improved. Most of the formulations use mainly zwitterionic, cationic or anionic lipids, PEG and/or cholesterol, which have different effects on stability, pharmacokinetics and delivery of the drug formulation. Clinical trials have shown that liposomes are pharmacologically and pharmacokinetically more efficient than drug-alone formulations in treating acute myeloid leukemia, hepatitis A, pain management, ovary, gastric breast and lung cancer, among others. Conclusion Liposomal formulations are less toxic than drugs alone and have better pharmacological parameters. Although they seem to be the first choice for drug delivery systems for various diseases, further research about dosage regimen regarding dose and time needs to be carried out.https://doi.org/10.1186/s12645-019-0055-yDrug delivery systemsNanoscaleLiposomal nanotechnologyRecent clinical trials
collection DOAJ
language English
format Article
sources DOAJ
author Esteban Beltrán-Gracia
Adolfo López-Camacho
Inocencio Higuera-Ciapara
Jesús B Velázquez-Fernández
Alba A Vallejo-Cardona
spellingShingle Esteban Beltrán-Gracia
Adolfo López-Camacho
Inocencio Higuera-Ciapara
Jesús B Velázquez-Fernández
Alba A Vallejo-Cardona
Nanomedicine review: clinical developments in liposomal applications
Cancer Nanotechnology
Drug delivery systems
Nanoscale
Liposomal nanotechnology
Recent clinical trials
author_facet Esteban Beltrán-Gracia
Adolfo López-Camacho
Inocencio Higuera-Ciapara
Jesús B Velázquez-Fernández
Alba A Vallejo-Cardona
author_sort Esteban Beltrán-Gracia
title Nanomedicine review: clinical developments in liposomal applications
title_short Nanomedicine review: clinical developments in liposomal applications
title_full Nanomedicine review: clinical developments in liposomal applications
title_fullStr Nanomedicine review: clinical developments in liposomal applications
title_full_unstemmed Nanomedicine review: clinical developments in liposomal applications
title_sort nanomedicine review: clinical developments in liposomal applications
publisher BMC
series Cancer Nanotechnology
issn 1868-6958
1868-6966
publishDate 2019-12-01
description Abstract Background In recent years, disease treatment has evolved strategies that require increase in pharmaceutical agent’s efficacy and selectivity while decreasing their toxicity in normal tissues. These requirements have led to the development of nanoscale liposome systems for drug release. This review focuses on lipid features, pharmacological properties of liposomal formulations and the clinical studies of their application. Main body Several lipids are available, but their properties could affect pharmacological or clinical efficiency of drug formulations. Many liposomal formulations have been developed and are currently on the market. Proper selection of lipid is essential for the pharmacological effect to be improved. Most of the formulations use mainly zwitterionic, cationic or anionic lipids, PEG and/or cholesterol, which have different effects on stability, pharmacokinetics and delivery of the drug formulation. Clinical trials have shown that liposomes are pharmacologically and pharmacokinetically more efficient than drug-alone formulations in treating acute myeloid leukemia, hepatitis A, pain management, ovary, gastric breast and lung cancer, among others. Conclusion Liposomal formulations are less toxic than drugs alone and have better pharmacological parameters. Although they seem to be the first choice for drug delivery systems for various diseases, further research about dosage regimen regarding dose and time needs to be carried out.
topic Drug delivery systems
Nanoscale
Liposomal nanotechnology
Recent clinical trials
url https://doi.org/10.1186/s12645-019-0055-y
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