Engineered Liposomes in Interventional Theranostics of Solid Tumors.


Journal

ACS biomaterials science & engineering
ISSN: 2373-9878
Titre abrégé: ACS Biomater Sci Eng
Pays: United States
ID NLM: 101654670

Informations de publication

Date de publication:
14 08 2023
Historique:
medline: 15 8 2023
pubmed: 14 7 2023
entrez: 14 7 2023
Statut: ppublish

Résumé

Engineered liposomal nanoparticles have unique characteristics as cargo carriers in cancer care and therapeutics. Liposomal theranostics have shown significant progress in preclinical and clinical cancer models in the past few years. Liposomal hybrid systems have not only been approved by the FDA but have also reached the market level. Nanosized liposomes are clinically proven systems for delivering multiple therapeutic as well as imaging agents to the target sites in (i) cancer theranostics of solid tumors, (ii) image-guided therapeutics, and (iii) combination therapeutic applications. The choice of diagnostics and therapeutics can intervene in the theranostics property of the engineered system. However, integrating imaging and therapeutics probes within lipid self-assembly "liposome" may compromise their overall theranostics performance. On the other hand, liposomal systems suffer from their fragile nature, site-selective tumor targeting, specific biodistribution and premature leakage of loaded cargo molecules before reaching the target site. Various engineering approaches, viz., grafting, conjugation, encapsulations, etc., have been investigated to overcome the aforementioned issues. It has been studied that surface-engineered liposomes demonstrate better tumor selectivity and improved therapeutic activity and retention in cells/or solid tumors. It should be noted that several other parameters like reproducibility, stability, smooth circulation, toxicity of vital organs, patient compliance, etc. must be addressed before using liposomal theranostics agents in solid tumors or clinical models. Herein, we have reviewed the importance and challenges of liposomal medicines in targeted cancer theranostics with their preclinical and clinical progress and a translational overview.

Identifiants

pubmed: 37450683
doi: 10.1021/acsbiomaterials.3c00510
doi:

Substances chimiques

Liposomes 0
Phospholipids 0

Types de publication

Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4527-4557

Auteurs

Nagavendra Kommineni (N)

Center for Biomedical Research, Population Council, New York, New York 10065, United States.

Ruchita Chaudhari (R)

School of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi 221005, India.

João Conde (J)

ToxOmics, NOVA Medical School, Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa; Lisboa 1169-056, Portugal.

Sedef Tamburaci (S)

Department of Chemical Engineering, Izmir Institute of Technology, Gulbahce Campus, Izmir 35430, Turkey.

Berivan Cecen (B)

Department of Biomedical Engineering, Rowan University, Glassboro, New Jersey 08028, United States.
Department of Mechanical Engineering, Rowan University, Glassboro, New Jersey 08028, United States.

Pranjal Chandra (P)

School of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi 221005, India.

Rajendra Prasad (R)

School of Biochemical Engineering, Indian Institute of Technology (BHU), Varanasi 221005, India.

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Classifications MeSH