In situ-gelling starch nanoparticle (SNP)/O-carboxymethyl chitosan (CMCh) nanoparticle network hydrogels for the intranasal delivery of an antipsychotic peptide

被引:47
作者
Majcher, Michael J. [1 ]
Babar, Ali [2 ]
Lofts, Andrew [2 ]
Leung, Ashlyn [1 ]
Li, Xiaoyun [1 ]
Abu-Hijleh, Fahed [3 ]
Smeets, Niels M. B. [1 ]
Mishra, Ram K. [3 ]
Hoare, Todd [1 ]
机构
[1] McMaster Univ, Dept Chem Engn, 1280 Main St, West Hamilton, ON L8S 4L8, Canada
[2] McMaster Univ, Sch Biomed Engn, 1280 Main St, West Hamilton, ON L8S 4L8, Canada
[3] McMaster Univ, Dept Psychiat & Behav Neurosci, 1280 Main St, West Hamilton, ON L8S 4L8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Nanoparticle networks; Starch; Hydrogel; Intranasal; Antipsychotics; Schizophrenia; In situ-gelling; Sprayable; RECEPTOR ALLOSTERIC MODULATOR; NEGATIVE SYMPTOMS; SOCIAL-INTERACTION; BRAIN DELIVERY; DRUG-DELIVERY; IN-VITRO; PART II; SCHIZOPHRENIA; PAOPA; NOSE;
D O I
10.1016/j.jconrel.2020.12.050
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Existing oral or injectable antipsychotic drug delivery strategies typically demonstrate low bioavailability to targeted brain regions, incentivizing the development of alternative delivery strategies. Delivery via the nasal cavity circumvents multiple barriers for reaching the brain but requires drug delivery vehicles with very specific properties to be effective. Herein, we report in situ-gelling and degradable bulk nanoparticle network hydrogels consisting of oxidized starch nanoparticles (SNPs) and carboxymethyl chitosan (CMCh) that enable intranasal delivery via spray, high nasal mucosal retention, and functional controlled release of the peptide drug PAOPA, a positive allosteric modulator of dopamine D2 receptor. PAOPA-loaded SNP-CMCh hydrogels can alleviate negative symptoms like behavioural abnormalities associated with schizophrenia (i.e. decreased social interaction time) for up to 72 h in an MK-801-induced pre-clinical rat model of schizophrenia at a low drug dosage (0.5 mg/kg); in comparison, conventional PAOPA administration via the intraperitoneal route requires twice the PAOPA dose to achieve a therapeutic effect that persists for only a few hours. This strategy offers potential for substantially decreasing re-administration frequencies and overall drug doses (and thus side-effects) of a range of potential antipsychotic drugs via a minimally-invasive administration route.
引用
收藏
页码:738 / 752
页数:15
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