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Strategies to improve the physicochemical properties of peptide-based drugs
被引:29
|作者:
Lee, Michelle Felicia
[1
]
Poh, Chit Laa
[1
]
机构:
[1] Sunway Univ, Ctr Virus & Vaccine Res, Sch Med & Life Sci, 5 Jalan Univ, Bandar Sunway 47500, Selangor, Malaysia
关键词:
chemical modifications;
drug delivery;
nanoparticles;
nanotechnology peptides;
CELL-PENETRATING PEPTIDES;
SOLID LIPID NANOPARTICLES;
BLOCK-COPOLYMER MICELLES;
ALPHA-AMINO-ACIDS;
ENDOMORPHIN-1;
ANALOGS;
MONOCLONAL-ANTIBODIES;
ENZYMATIC-HYDROLYSIS;
SILVER NANOPARTICLES;
THERAPEUTIC AGENTS;
GAMMA-PEPTIDES;
D O I:
10.1007/s11095-023-03486-0
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Peptides are a rapid-growing class of therapeutics with unique and desirable physicochemical properties. Due to disadvantages such as low membrane permeability and susceptibility to proteolytic degradation, peptide-based drugs have limited bioavailability, a short half-life, and rapid in vivo elimination. Various strategies can be applied to improve the physicochemical properties of peptide-based drugs to overcome limitations such as limited tissue residence time, metabolic instability, and low permeability. Applied strategies including backbone modifications, side chain modifications, conjugation with polymers, modification of peptide termini, fusion to albumin, conjugation with the Fc portion of antibodies, cyclization, stapled peptides, pseudopeptides, cell-penetrating peptide conjugates, conjugation with lipids, and encapsulation in nanocarriers are discussed.
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页码:617 / 632
页数:16
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