PEGylated Nanoliposomes Potentiated Oral Combination Therapy for Effective Cancer Treatment.


Journal

Current drug delivery
ISSN: 1875-5704
Titre abrégé: Curr Drug Deliv
Pays: United Arab Emirates
ID NLM: 101208455

Informations de publication

Date de publication:
2020
Historique:
received: 21 03 2020
revised: 23 04 2020
accepted: 24 06 2020
pubmed: 28 7 2020
medline: 3 8 2021
entrez: 28 7 2020
Statut: ppublish

Résumé

The conventional treatment regimen for cancer with a single chemotherapeutic agent is far behind the clinical expectations due to the complexity of cancer biology and is also associated with poor Quality of Life (QOL) due to off-site toxicity and multidrug resistance. In recent years, nanopotentiated combination therapy has shown significant improvement in cancer treatment via a synergistic approach. However, being synthetic in nature, nanocarriers have been associated with the activation of the Complement (C) activation system resulting in serious hypersensitivity reactions known as CActivation Related Pseudoallergy (CARPA) effect once given via intravenous injection. On the other hand, nanopotentiated oral drug delivery offers several advantages for the effective and safe delivery of the drug to the target site. This hypothesis aims to put forward wherein Exemestane (chemotherapeutic agent) and lycopene (herbal bioactive) co-laden into PEGylated liposomes and delivered to the breast cancer via the oral route. PEGylation of the liposomes would prevent both molecules from the harsh microenvironment of the Gastrointestinal Tract (GIT) and would eventually promote their intestinal absorption via the lymphatic pathway to the systemic circulation. Lycopene being a potent antioxidant and anti-cancer herbal bioactive would promote the therapeutic efficacy of the Exemestane via a synergistic approach. This nanopotentiated oral combination therapy would pave the path for the safe and effective treatment of cancer.

Identifiants

pubmed: 32713341
pii: CDD-EPUB-108455
doi: 10.2174/1567201817666200724170708
doi:

Substances chimiques

Androstadienes 0
Aromatase Inhibitors 0
Liposomes 0
Polyethylene Glycols 3WJQ0SDW1A
exemestane NY22HMQ4BX
Lycopene SB0N2N0WV6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

728-735

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Archu Singh (A)

Department of Pharmaceutics, School of Pharmaceutical Education & Research, Jamia Hamdard, New Delhi-110062, India.

Yub Raj Neupane (YR)

Department of Pharmacy, National University of Singapore, 117559, Singapore.

Bharti Mangla (B)

Department of Pharmaceutics, School of Pharmaceutical Education & Research, Jamia Hamdard, New Delhi-110062, India.

Sadat Shafi (S)

Pharmaceutical Medicine, Department of Pharmacology, School of Pharmaceutical Education and Research, Jamia Hamdard, New Delhi-110062, India.

Kanchan Kohli (K)

Department of Pharmaceutics, School of Pharmaceutical Education & Research, Jamia Hamdard, New Delhi-110062, India.

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Classifications MeSH