4.7 Review

Preclinical Nanomedicines for Polyglutamine-Based Neurodegenerative Diseases

期刊

MOLECULAR PHARMACEUTICS
卷 18, 期 2, 页码 610-626

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.molpharmaceut.0c00506

关键词

neurodegenerative diseases; Huntington's disease; polyglutamine; brain delivery; nanoparticles; nanomedicine

资金

  1. Research Grants Council (RGC) of Hong Kong [14302916, ACUHK401/14]
  2. Gerald Choa Neuroscience Centre and Chow Yuk Ho Technology Centre for Innovative Medicine at The Chinese University of Hong Kong (CUHK)
  3. CUHK Vice-Chancellor Discretionary Fund [VCF2014011, EC/2017/010, EC/2017/012]
  4. Croucher Foundation
  5. Hong Kong Ph.D. Fellowship by the RGC

向作者/读者索取更多资源

Polyglutamine diseases are inheritable progressive neurodegenerative disorders lacking disease-modifying therapeutic interventions. Nanoparticles offer potential for improved drug delivery to the brain, with promising preclinical applications in treating polyQ diseases. The future of nanomedicines for polyQ diseases appears promising with developments in inorganic nanoparticles and novel drug candidates.
Polyglutamine (polyQ) diseases, such as Huntington's disease and several types of spinocerebellar ataxias, are dominantly inherited progressive neurodegenerative disorders and characterized by the presence of expanded CAG trinucleotide repeats in the respective disease locus of the patient genomes. Patients with polyQ diseases currently need to rely on symptom-relieving treatments because disease-modifying therapeutic interventions remain scarce. Many disease-modifying therapeutic agents are now under clinical testing for treating polyQ diseases, but their delivery to the brain is often too invasive (e.g., intracranial injection) or inefficient, owing to in vivo degradation and clearance by physiological barriers (e.g., oral and intravenous administration). Nanoparticles provide a feasible solution for improving drug delivery to the brain, as evidenced by an increasing number of preclinical studies that document the efficacy of nanomedicines for polyQ diseases over the past 5-6 years. In this review, we present the pathogenic mechanisms of polyQ diseases, the common animal models of polyQ diseases for evaluating the efficacy of nanomedicines, and the common administration routes for delivering nanoparticles to the brain. Next, we summarize the recent preclinical applications of nanomedicines for treating polyQ diseases and improving neurological conditions in vivo, placing emphasis on antisense oligonucleotides, small peptide inhibitors, and small molecules as the disease-modifying agents. We conclude with our perspectives of the burgeoning field of nanomedicines for polyQ diseases, including the use of inorganic nanoparticles and potential drugs as next-generation nanomedicines, development of higher-order animal models of polyQ diseases, and importance of brain-nano interactions.

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