A decade's worth of impact: Dox loaded liposomes in anticancer activity

Clinically approved therapeutics associated with cancer are limited to mostly chemotherapy, surgery and radiotherapy in spite of the advancements in the biomedical field. Due to the cardiotoxicity and uncountable side effects brought by the prevailing treatment strategies, demands are growing for ta...

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Veröffentlicht in:Materials today advances 2022-12, Vol.16, p.100313, Article 100313
Hauptverfasser: Ghosh, Puja, Tiwari, Himja, Lakkakula, Jaya, Roy, Arpita, Emran, Talha Bin, Rashid, Summya, Alghamdi, Saad, Rajab, Bodour S., Almehmadi, Mazen, Allahyani, Mamdouh, Aljuaid, Abdulelah, Alsaiari, Ahad Amer, Sharma, Rohit, Babalghith, Ahmad O.
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Sprache:eng
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Zusammenfassung:Clinically approved therapeutics associated with cancer are limited to mostly chemotherapy, surgery and radiotherapy in spite of the advancements in the biomedical field. Due to the cardiotoxicity and uncountable side effects brought by the prevailing treatment strategies, demands are growing for targeted drug delivery using nanomaterials. For this the most commonly used drug, doxorubicin (DOX) is encapsulated within several type of nanovesicles to observe their anticancer activity. Among them, DOX encapsulated liposomes gained popularity because of their clinical success and lower toxicity. To enhance their efficiency and site specific delivery, attempts are made to modify the liposomes by combining them with peptides, aptamers, antibodies etc to develop pH, thermal, UV-sensitive and electro-magnetic liposomal nanocarriers for controlled drug release. The novel strategies for the treatment of Breast, Lung, Liver, Pancreatic, Prostate, Ovarian, Cervical, Blood, Brain and Colon cancer using modified liposomes encapsulating DOX are illustrated in this review. [Display omitted] •Liposomal nanovesicles for the delivery of Doxorubicin are highlighted.•Liposomes for treatment of various cancers are explored.•Different forms of liposomes in combination with various materials are presented.
ISSN:2590-0498
2590-0498
DOI:10.1016/j.mtadv.2022.100313