Curcumin-loaded self-nanomicellizing solid dispersion system: part II: in vivo safety and efficacy assessment against behavior deficit in Alzheimer disease.

Ankit Parikh, Krishna Kathawala, Jintao Li, Chi Chen, Zhengnan Shan, Xia Cao, Xin-Fu Zhou, Sanjay Garg
Author Information
  1. Ankit Parikh: School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, 5000, Australia.
  2. Krishna Kathawala: School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, 5000, Australia.
  3. Jintao Li: School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, 5000, Australia.
  4. Chi Chen: School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, 5000, Australia.
  5. Zhengnan Shan: School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, 5000, Australia.
  6. Xia Cao: Central laboratory, Second Affiliated Hospital of Kunming Medical University, Kunming, 650101, Yunnan Province, China.
  7. Xin-Fu Zhou: School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, 5000, Australia. Xin-Fu.Zhou@unisa.edu.au.
  8. Sanjay Garg: School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, 5000, Australia. Sanjay.Garg@unisa.edu.au.

Abstract

Curcumin (CUR), a natural polyphenolic compound, is considered as one of the most potential candidates against Alzheimer disease (AD) by targeting multiple pathologies such as amyloid-beta, tau phosphorylation, and oxidative stress. Poor physicochemical profile and oral bioavailability (BA) are the major contributors to its failure in clinical trials. Lack of success in numerous drug clinical trials for the treatment of AD urges the need of repositioning of CUR. To overcome its limitation and enhance oral BA, Novel CUR Formulation (NCF) was developed using self-nanomicellizing solid dispersion strategy which displayed 117-fold enhancement in oral BA of CUR. NCF was tested using SH-SY5Y695 APP human neuroblastoma cell line against the cytotoxicity induced by copper metal ion, HO, and Aβ42 oligomer and compared with CUR control. The safety and efficacy of NCF on mice AD-like behavioral deficits (open field, novel objective recognition, Y-maze, and Morris water maze tests) were assessed in transgenic AD (APPSwe/PS1deE9) mice model. In SH-SY5Y695 APP human neuroblastoma cell line, NCF showed better safety and efficacy against the cytotoxicity due to the significantly enhancement of cellular uptake. It not only prevents the deterioration of cognitive functions of the aged APPSwe/PS1deE9 mice during aging but also reverses the cognitive functions to their much younger age which is also better than the currently available approved options. Moreover, NCF was proved as well tolerated with no appearance of any significant toxicity via oral administration. The results of the study demonstrated the potential of NCF to improve the efficacy of CUR without compromising its safety profile, and pave the way for clinical development for AD.

Keywords

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MeSH Term

Administration, Oral
Alzheimer Disease
Amyloid beta-Peptides
Animals
Cell Line
Cognitive Dysfunction
Copper
Curcumin
Disease Models, Animal
Drug Compounding
Humans
Hydrogen Peroxide
Male
Mice
Mice, Transgenic
Micelles
Nanostructures
Peptide Fragments

Chemicals

Amyloid beta-Peptides
Micelles
Peptide Fragments
amyloid beta-protein (1-42)
Copper
Hydrogen Peroxide
Curcumin

Word Cloud

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