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Construction of Cyclic Cell-Penetrating Peptides for Enhanced Penetration of Biological Barriers
Published on: September 19, 2022
Cell-penetrating peptides (CPPs)-engineered PLGA nanocarriers for enhanced drug delivery: Uptake mechanisms,
Atefeh Malek-Khatabi1, Milad Rahimzadegan2, Malihe Sadat Razavi3
1Center for Advanced Biomaterials for Health Care (CABHC), Italian Institute of Technology, Napoli, Italy; Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Abstract:
One major barrier inhibiting most pharmaceutical administrations' effectiveness is the cellular membrane's insufficient permeability. Cell-penetrating peptides (CPPs) are extensively identified as effective biological carriers that can pass through this natural barrier and transport the CPPs-conjugated therapeutic agents into cells. In this line, CPPs-assisted delivery systems have become one of the most popular methods for internalizing nanoparticles (NPs). Recently, CPPs-functionalized PLGA-derived nanocarriers have attracted exceptional attention because of their distinctive features that make them highly appealing for use in next-generation drug delivery systems (DDS). CPPs-conjugated PLGA NPs have demonstrated promise as therapeutic agents in a range of medical fields. This review article summarizes the current development of the CPPs/PLGA nanocarriers. After that, we explore their various challenges and optimization techniques. Finally, future prospects and challenges of CPPs/PLGA nanocarriers are mentioned concisely.
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