TY - JOUR
T1 - Highlights on Cell-Penetrating Peptides and Polymer-Lipid Hybrid Nanoparticle
T2 - Overview and Therapeutic Applications for Targeted Anticancer Therapy
AU - Bangera, Pragathi Devanand
AU - Kara, Divya Dhatri
AU - Tanvi, Katikala
AU - Tippavajhala, Vamshi Krishna
AU - Rathnanand, Mahalaxmi
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/6
Y1 - 2023/6
N2 - Polymer-lipid hybrid nanoparticles (PLHNs) have been widely used as a vehicle for carrying anticancer owing to its unique framework of polymer and lipid combining and giving the maximum advantages over the lipid and polymer nanoparticle drug delivery system. Surface modification of PLHNs aids in improved targeting and active delivery of the encapsulated drug. Therefore, surface modification of the PLHNs with the cell-penetrating peptide is explored by many researchers and is explained in this review. Cell-penetrating peptides (CPPs) are made up of few amino acid sequence and act by disrupting the cell membrane and transferring the cargos into the cell. Ideally, we can say that CPPs are peptide chains which are cell specific and are biocompatible, noninvasive type of delivery vehicle which can transport siRNA, protein, peptides, macromolecules, pDNA, etc. into the cell effectively. Therefore, this review focuses on the structure, type, and method of preparation of PLHNs also about the uptake mechanism of CPPs and concludes with the therapeutic application of PLHNs surface modified with the CPPs and their theranostics. Graphical Abstract: [Figure not available: see fulltext.]
AB - Polymer-lipid hybrid nanoparticles (PLHNs) have been widely used as a vehicle for carrying anticancer owing to its unique framework of polymer and lipid combining and giving the maximum advantages over the lipid and polymer nanoparticle drug delivery system. Surface modification of PLHNs aids in improved targeting and active delivery of the encapsulated drug. Therefore, surface modification of the PLHNs with the cell-penetrating peptide is explored by many researchers and is explained in this review. Cell-penetrating peptides (CPPs) are made up of few amino acid sequence and act by disrupting the cell membrane and transferring the cargos into the cell. Ideally, we can say that CPPs are peptide chains which are cell specific and are biocompatible, noninvasive type of delivery vehicle which can transport siRNA, protein, peptides, macromolecules, pDNA, etc. into the cell effectively. Therefore, this review focuses on the structure, type, and method of preparation of PLHNs also about the uptake mechanism of CPPs and concludes with the therapeutic application of PLHNs surface modified with the CPPs and their theranostics. Graphical Abstract: [Figure not available: see fulltext.]
UR - http://www.scopus.com/inward/record.url?scp=85160137183&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85160137183&partnerID=8YFLogxK
U2 - 10.1208/s12249-023-02576-x
DO - 10.1208/s12249-023-02576-x
M3 - Review article
C2 - 37225901
AN - SCOPUS:85160137183
SN - 1530-9932
VL - 24
JO - AAPS PharmSciTech
JF - AAPS PharmSciTech
IS - 5
M1 - 124
ER -