Liposomal Nanosystems in Rheumatoid Arthritis

Rheumatoid arthritis (RA) is an autoimmune disease that affects the joints and results in reduced patient quality of life due to its chronic nature and several comorbidities. RA is also associated with a high socioeconomic burden. Currently, several available therapies minimize symptoms and prevent...

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Main Authors: Margarida Ferreira-Silva, Catarina Faria-Silva, Pedro Viana Baptista, Eduarda Fernandes, Alexandra Ramos Fernandes, Maria Luísa Corvo
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/13/4/454
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author Margarida Ferreira-Silva
Catarina Faria-Silva
Pedro Viana Baptista
Eduarda Fernandes
Alexandra Ramos Fernandes
Maria Luísa Corvo
author_facet Margarida Ferreira-Silva
Catarina Faria-Silva
Pedro Viana Baptista
Eduarda Fernandes
Alexandra Ramos Fernandes
Maria Luísa Corvo
author_sort Margarida Ferreira-Silva
collection DOAJ
description Rheumatoid arthritis (RA) is an autoimmune disease that affects the joints and results in reduced patient quality of life due to its chronic nature and several comorbidities. RA is also associated with a high socioeconomic burden. Currently, several available therapies minimize symptoms and prevent disease progression. However, more effective treatments are needed due to current therapies’ severe side-effects, especially under long-term use. Drug delivery systems have demonstrated their clinical importance—with several nanocarriers present in the market—due to their capacity to improve therapeutic drug index, for instance, by enabling passive or active targeting. The first to achieve market authorization were liposomes that still represent a considerable part of approved delivery systems. In this manuscript, we review the role of liposomes in RA treatment, address preclinical studies and clinical trials, and discuss factors that could hamper a successful clinical translation. We also suggest some alterations that could potentially improve their progression to the market.
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spelling doaj.art-89c7603ff1244cd0a996580cb3c8b7212023-11-21T13:02:43ZengMDPI AGPharmaceutics1999-49232021-03-0113445410.3390/pharmaceutics13040454Liposomal Nanosystems in Rheumatoid ArthritisMargarida Ferreira-Silva0Catarina Faria-Silva1Pedro Viana Baptista2Eduarda Fernandes3Alexandra Ramos Fernandes4Maria Luísa Corvo5Instituto de Investigação do Medicamento (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisbon, PortugalInstituto de Investigação do Medicamento (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisbon, PortugalUnidade de Ciências Biomoleculares Aplicadas UCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Campus de Caparica, 2829-516 Caparica, PortugalAssociated Laboratory for Green Chemistry of the Network of Chemistry and Technology (LAQV, REQUIMTE), Laboratory of Applied Chemistry, Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, Rua de Jorge Viterbo Ferreira, 228, 4050-313 Porto, PortugalUnidade de Ciências Biomoleculares Aplicadas UCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Campus de Caparica, 2829-516 Caparica, PortugalInstituto de Investigação do Medicamento (iMed.ULisboa), Faculdade de Farmácia, Universidade de Lisboa, Av. Prof. Gama Pinto, 1649-003 Lisbon, PortugalRheumatoid arthritis (RA) is an autoimmune disease that affects the joints and results in reduced patient quality of life due to its chronic nature and several comorbidities. RA is also associated with a high socioeconomic burden. Currently, several available therapies minimize symptoms and prevent disease progression. However, more effective treatments are needed due to current therapies’ severe side-effects, especially under long-term use. Drug delivery systems have demonstrated their clinical importance—with several nanocarriers present in the market—due to their capacity to improve therapeutic drug index, for instance, by enabling passive or active targeting. The first to achieve market authorization were liposomes that still represent a considerable part of approved delivery systems. In this manuscript, we review the role of liposomes in RA treatment, address preclinical studies and clinical trials, and discuss factors that could hamper a successful clinical translation. We also suggest some alterations that could potentially improve their progression to the market.https://www.mdpi.com/1999-4923/13/4/454rheumatoid arthritisdrug delivery nanosystemsliposomespassive targetingactive targeting
spellingShingle Margarida Ferreira-Silva
Catarina Faria-Silva
Pedro Viana Baptista
Eduarda Fernandes
Alexandra Ramos Fernandes
Maria Luísa Corvo
Liposomal Nanosystems in Rheumatoid Arthritis
Pharmaceutics
rheumatoid arthritis
drug delivery nanosystems
liposomes
passive targeting
active targeting
title Liposomal Nanosystems in Rheumatoid Arthritis
title_full Liposomal Nanosystems in Rheumatoid Arthritis
title_fullStr Liposomal Nanosystems in Rheumatoid Arthritis
title_full_unstemmed Liposomal Nanosystems in Rheumatoid Arthritis
title_short Liposomal Nanosystems in Rheumatoid Arthritis
title_sort liposomal nanosystems in rheumatoid arthritis
topic rheumatoid arthritis
drug delivery nanosystems
liposomes
passive targeting
active targeting
url https://www.mdpi.com/1999-4923/13/4/454
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AT eduardafernandes liposomalnanosystemsinrheumatoidarthritis
AT alexandraramosfernandes liposomalnanosystemsinrheumatoidarthritis
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