Synthetic Anti-Cocaine Nanoaccine Successfully Prevents Cocaine-Induced Hyperlocomotion

被引:4
|
作者
Madge, Harrison Y. R. [1 ]
Alexander, Suzy [2 ,3 ]
Azuar, Armira [1 ,4 ]
Zhang, Jiahui [1 ,4 ]
Koirala, Prashamsa [1 ,4 ]
Burne, Thomas H. [2 ,3 ]
Toth, Istvan [1 ,4 ]
Stephenson, Rachel J. [1 ]
机构
[1] Univ Queensland, Sch Chem & Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Queensland, Queensland Brain Inst, Brisbane, Qld 4072, Australia
[3] Queensland Ctr Mental Hlth Res, Wacol, Qld 4076, Australia
[4] Univ Queensland, Sch Pharm, Brisbane, Qld 4072, Australia
基金
英国医学研究理事会;
关键词
INDUCED EPITOPIC SUPPRESSION; VACCINE; CARRIER; ADJUVANT; POTENCY; MF59;
D O I
10.1021/acs.jmedchem.3c00889
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cocaine is one of the most widely used and increasingly popular illicit psychoactive drugs. Unlike other commonly used substances of abuse, cocaine has no pharmacological therapies to treat addiction or aid in rehabilitation. Immunopharmacology has long been touted as a possible avenue to develop effective anticocaine therapies; however, lack of efficacy and designs which are not consistent with simple large-scale production have hindered vaccine translation. We have designed and synthesized a peptide-based anti-cocaine immunogen which we have shown is capable of inducing physiologically relevant immune responses in mice as part of a self-adjuvanting delivery system or in combination with the human-approved commercial adjuvant MF59. We have demonstrated that immunization with the reported vaccine elicits high titers of anti-cocaine IgG and prevents cocaine-induced hyperlocomotion in an in vivo murine model. This peptide-hapten immunogen along with self-adjuvanting liposomal-based delivery system provides a platform for the development of effective anti-drug vaccines.
引用
收藏
页码:12407 / 12419
页数:13
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