Nano drug-delivery systems for management of AIDS: liposomes, dendrimers, gold and silver nanoparticles.


Journal

Nanomedicine (London, England)
ISSN: 1748-6963
Titre abrégé: Nanomedicine (Lond)
Pays: England
ID NLM: 101278111

Informations de publication

Date de publication:
02 2023
Historique:
pmc-release: 01 02 2024
medline: 12 5 2023
pubmed: 1 5 2023
entrez: 1 5 2023
Statut: ppublish

Résumé

AIDS causes increasing mortality every year. With advancements in nanomedicine, different nanomaterials (NMs) have been applied to treat AIDS and overcome its limitations. Among different NMs, nanoparticles (NPs) can act as nanocarriers due to their enhanced solubility, sustained release, targeting abilities and facilitation of drug-dose reductions. This review discusses recent advancements in therapeutics for AIDS/HIV using various NMs, mainly focused on three classifications: polymeric, liposomal and inorganic NMs. Polymeric dendrimers, polyethylenimine-NPs, poly(lactic-co-glycolic acid)-NPs, chitosan and the use of liposomal-based delivery systems and inorganic NPs, including gold and silver NPs, are explored. Recent advances, current challenges and future perspectives on the use of these NMs for better management of HIV/AIDS are also discussed. AIDS is a disease affecting many worldwide. Since it is difficult to cure AIDS, new therapies have been developed. Tiny materials called nanoparticles with promising features are used to carry different drugs to relevant organs in the body. There are various nanoparticles with different textures and shapes used in AIDS therapy. Branched nanoparticles, nanoparticles with repetitive building blocks and metal-based nanoparticles are three commonly used nanoparticles in AIDS treatment that are studied in this review. These tiny materials can find the exact place in the body to deliver drugs. They can also reduce the side effects of anti-AIDS drugs and help patients use fewer drugs while getting the same or better results.

Autres résumés

Type: plain-language-summary (eng)
AIDS is a disease affecting many worldwide. Since it is difficult to cure AIDS, new therapies have been developed. Tiny materials called nanoparticles with promising features are used to carry different drugs to relevant organs in the body. There are various nanoparticles with different textures and shapes used in AIDS therapy. Branched nanoparticles, nanoparticles with repetitive building blocks and metal-based nanoparticles are three commonly used nanoparticles in AIDS treatment that are studied in this review. These tiny materials can find the exact place in the body to deliver drugs. They can also reduce the side effects of anti-AIDS drugs and help patients use fewer drugs while getting the same or better results.

Identifiants

pubmed: 37125616
doi: 10.2217/nnm-2022-0248
pmc: PMC10242436
doi:

Substances chimiques

Liposomes 0
Dendrimers 0
Silver 3M4G523W1G
Nanoparticle Drug Delivery System 0
Gold 7440-57-5
Polymers 0

Types de publication

Journal Article Review Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

279-302

Subventions

Organisme : NIBIB NIH HHS
ID : T32 EB009035
Pays : United States

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Auteurs

Fateme Davarani Asl (FD)

Department of Medical Biotechnology, School of Advanced Technologies, Shahrekord University of Medical Sciences, Shahrekord, 88138-33435, Iran.

Marziyeh Mousazadeh (M)

Department of Nanobiotechnology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, 14115-154, Iran.

Shirinsadat Taji (S)

Department of Nanobiotechnology, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, 14115-154, Iran.
Institute for Genetics, University of Cologne, Cologne, D-50674, Germany.

Abbas Bahmani (A)

Institute for Nanoscience & Nanotechnology (INST), Sharif University of Technology, Tehran, 14588-89694, Iran.

Patricia Khashayar (P)

Center for Microsystems Technology, Imec & Ghent University, Ghent, 9050, Belgium.

Mostafa Azimzadeh (M)

Medical Nanotechnology & Tissue Engineering Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, 89195-999, Iran.

Ebrahim Mostafavi (E)

Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

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