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Advances in functional lipid nanoparticles: from drug delivery platforms to clinical applications
被引:15
|作者:
Dhayalan, Manikandan
[1
,10
]
Wang, Wei
[2
]
Riyaz, S. U. Mohammed
[1
,3
]
Dinesh, Rakshi Anuja
[11
]
Shanmugam, Jayashree
[4
]
Irudayaraj, Santiagu Stephen
[5
]
Stalin, Antony
[6
]
Giri, Jayant
[7
]
Mallik, Saurav
[8
]
Hu, Ruifeng
[9
]
机构:
[1] Saveetha Univ, Saveetha Dent Coll & Hosp, Saveetha Inst Med & Tech Sci, Dept Prosthodont, Chennai 600077, Tamil Nadu, India
[2] Beidahuang Ind Grp Gen Hosp, Harbin 150001, Peoples R China
[3] Islamiah Coll Autonomous, PG & Res Dept Biotechnol, Vaniyambadi 635752, Tamil Nadu, India
[4] Sathyabama Inst Sci & Technol, Dept Biotechnol, Chennai, Tamil Nadu, India
[5] St Xaviers Coll, Dumka 814110, Jharkhand, India
[6] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Peoples R China
[7] Yeshwantrao Chavan Coll Engn, Dept Mech Engn, Nagpur, India
[8] Harvard TH Chan Sch Publ Hlth, Dept Environm Hlth, Boston, MA 02115 USA
[9] Harvard Med Sch, Dept Neurol, Boston, MA USA
[10] Chulalongkorn Univ, Coll Publ Hlth Sci CPHS, 254 Phyathai Rd, Bangkok 10330, Thailand
[11] Univ Queensland, Sch Chem & Mol Biosci, St Lucia, Qld 4072, Australia
来源:
关键词:
Rapamycin-coated lipid;
Lipid nanoparticles;
Nucleic acid medications;
Biocompatibility;
Nontoxicity;
Targeted delivery;
CELL-PENETRATING PEPTIDE;
MESSENGER-RNA VACCINES;
NERVOUS-SYSTEM CNS;
TARGETED DELIVERY;
IN-VITRO;
AMPHOTERICIN-B;
SENSITIZES GLIOBLASTOMA;
THERAPEUTIC DELIVERY;
LOADED LIPOSOMES;
APOLIPOPROTEIN-E;
D O I:
10.1007/s13205-023-03901-8
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Since Doxil's first clinical approval in 1995, lipid nanoparticles have garnered great interest and shown exceptional therapeutic efficacy. It is clear from the licensure of two RNA treatments and the mRNA-COVID-19 vaccination that lipid nanoparticles have immense potential for delivering nucleic acids. The review begins with a list of lipid nanoparticle types, such as liposomes and solid lipid nanoparticles. Then it moves on to the earliest lipid nanoparticle forms, outlining how lipid is used in a variety of industries and how it is used as a versatile nanocarrier platform. Lipid nanoparticles must then be functionally modified. Various approaches have been proposed for the synthesis of lipid nanoparticles, such as High-Pressure Homogenization (HPH), microemulsion methods, solvent-based emulsification techniques, solvent injection, phase reversal, and membrane contractors. High-pressure homogenization is the most commonly used method. All of the methods listed above follow four basic steps, as depicted in the flowchart below. Out of these four steps, the process of dispersing lipids in an aqueous medium to produce liposomes is the most unpredictable step. A short outline of the characterization of lipid nanoparticles follows discussions of applications for the trapping and transporting of various small molecules. It highlights the use of rapamycin-coated lipid nanoparticles in glioblastoma and how lipid nanoparticles function as a conjugator in the delivery of anticancer-targeting nucleic acids. High biocompatibility, ease of production, scalability, non-toxicity, and tailored distribution are just a meager of the enticing allowances of using lipid nanoparticles as drug delivery vehicles. Due to the present constraints in drug delivery, more research is required to utterly realize the potential of lipid nanoparticles for possible clinical and therapeutic purposes.
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页数:28
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