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

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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, H2O2, 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.

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References

  1. Roberson ED, Mucke L. 100 years and counting: prospects for defeating Alzheimer’s disease. Science. 2006;314(5800):781–4. https://doi.org/10.1126/science.1132813.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  2. Mangialasche F, Solomon A, Winblad B, Mecocci P, Kivipelto M. Alzheimer’s disease: clinical trials and drug development. The Lancet Neurology. 2010;9(7):702–16. https://doi.org/10.1016/S1474-4422(10)70119-8.

    Article  PubMed  CAS  Google Scholar 

  3. Iqbal K, Liu F, Gong CX. Alzheimer disease therapeutics: focus on the disease and not just plaques and tangles. Biochem Pharmacol. 2014;88:631–9. https://doi.org/10.1016/j.bcp.2014.01.002.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  4. Schneider LS, Mangialasche F, Andreasen N, Feldman H, Giacobini E, Jones R, et al. Clinical trials and late-stage drug development for Alzheimer’s disease: an appraisal from 1984 to 2014. J Intern Med. 2014;275(3):251–83. https://doi.org/10.1111/joim.12191.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  5. Mishra S, Palanivelu K. The effect of curcumin (turmeric) on Alzheimer’s disease: an overview. Annals of Indian Academy of Neurology. 2008;11(1):13–9. https://doi.org/10.4103/0972-2327.40220.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Zeng YQ, Wang YJ, Zhou XF. Effects of (−)epicatechin on the pathology of APP/PS1 transgenic mice. Front Neurol. 2014;5:69. https://doi.org/10.3389/fneur.2014.00069.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Wang YJ, Thomas P, Zhong JH, Bi FF, Kosaraju S, Pollard A, et al. Consumption of grape seed extract prevents amyloid-beta deposition and attenuates inflammation in brain of an Alzheimer’s disease mouse. Neurotox Res. 2009;15(1):3–14. https://doi.org/10.1007/s12640-009-9000-x.

    Article  PubMed  CAS  Google Scholar 

  8. Ringman JM, Frautschy SA, Teng E, Begum AN, Bardens J, Beigi M, et al. Oral curcumin for Alzheimer’s disease: tolerability and efficacy in a 24-week randomized, double blind, placebo-controlled study. Alzheimers Res Ther. 2012;4(5):43. https://doi.org/10.1186/alzrt146.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  9. Mecocci P, Polidori MC. Antioxidant clinical trials in mild cognitive impairment and Alzheimer’s disease. Biochim Biophys Acta. 2012;1822(5):631–8. https://doi.org/10.1016/j.bbadis.2011.10.006.

    Article  PubMed  CAS  Google Scholar 

  10. Anand P, Kunnumakkara AB, Newman RA, Aggarwal BB. Bioavailability of curcumin: problems and promises. Mol Pharm. 2007;4(6):807–18. https://doi.org/10.1021/mp700113r.

    Article  PubMed  CAS  Google Scholar 

  11. Parikh A, Kathawala K, Tan CC, Garg S, Zhou XF. Development of a novel oral delivery system of edaravone for enhancing bioavailability. Int J Pharm. 2016;515(1–2):490–500. https://doi.org/10.1016/j.ijpharm.2016.10.052.

    Article  PubMed  CAS  Google Scholar 

  12. Parikh A, Kathawala K, Tan CC, Garg S, Zhou XF. Lipid-based nanosystem of edaravone: development, optimization, characterization and in vitro/in vivo evaluation. Drug delivery. 2017;24(1):962–78. https://doi.org/10.1080/10717544.2017.1337825.

    Article  PubMed  CAS  Google Scholar 

  13. Parikh A, Kathawala K, Tan CC, Garg S, Zhou X-F. Self-nanomicellizing solid dispersion of edaravone: part I; oral bioavailability improvement. Drug design, development and therapy. 2018;12:2051–69. https://doi.org/10.2147/dddt.s161940.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Parikh A, Kathawala K, Song Y, Zhou XF, Garg S. Curcumin-loaded self-nanomicellizing solid dispersion system: part I: development, optimization, characterization, and oral bioavailability. Drug delivery and translational research. 2018; https://doi.org/10.1007/s13346-018-0543-3.

  15. Parikh A, Kathawala K, Li J, Chen C, Shan Z, Cao X, et al. Self-nanomicellizing solid dispersion of edaravone: part II: in vivo assessment of efficacy against behavior deficits and safety in Alzheimer’s disease model. Drug design, development and therapy. 2018;12:2111–28. https://doi.org/10.2147/dddt.s161944.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Teixeira CC, Mendonca LM, Bergamaschi MM, Queiroz RH, Souza GE, Antunes LM, et al. Microparticles containing curcumin solid dispersion: stability. Bioavailability and anti-inflammatory activity AAPS pharmSciTech. 2016;17(2):252–61. https://doi.org/10.1208/s12249-015-0337-6.

    Article  PubMed  CAS  Google Scholar 

  17. Wang C, Ma C, Wu Z, Liang H, Yan P, Song J, et al. Enhanced bioavailability and anticancer effect of curcumin-loaded electrospun nanofiber: in vitro and in vivo study. Nanoscale Res Lett. 2015;10(1):439. https://doi.org/10.1186/s11671-015-1146-2.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  18. Patil S, Choudhary B, Rathore A, Roy K, Mahadik K. Enhanced oral bioavailability and anticancer activity of novel curcumin loaded mixed micelles in human lung cancer cells. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2015;22(12):1103–11. https://doi.org/10.1016/j.phymed.2015.08.006.

    Article  CAS  Google Scholar 

  19. Hagl S, Heinrich M, Kocher A, Schiborr C, Frank J, Eckert GP. Curcumin micelles improve mitochondrial function in a mouse model of Alzheimer’s disease. The Journal of Prevention of Alzheimer’s Disease. 2014;1(2):80–3.

    PubMed  CAS  Google Scholar 

  20. Buckholtz NS, Ryan LM, Petanceska S, Refolo LM. NIA commentary: translational issues in Alzheimer’s disease drug development. Neuropsychopharmacology: official publication of the American College of Neuropsychopharmacology. 2012;37(1):284–6. https://doi.org/10.1038/npp.2011.116.

    Article  Google Scholar 

  21. LaFerla FM, Green KN. Animal models of Alzheimer disease. Cold Spring Harbor perspectives in medicine. 2012; 2(11). https://doi.org/10.1101/cshperspect.a006320.

  22. Saraceno C, Musardo S, Marcello E, Pelucchi S, Di Luca M. Modeling Alzheimer’s disease: from past to future. Front Pharmacol. 2013;4:77. https://doi.org/10.3389/fphar.2013.00077.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Russo P, Kisialiou A, Lamonaca P, Moroni R, Prinzi G, Fini M. New drugs from marine organisms in Alzheimer’s disease. Marine drugs. 2015;14(1):5. https://doi.org/10.3390/md14010005.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  24. Wang YJ, Pollard A, Zhong JH, Dong XY, Wu XB, Zhou HD, et al. Intramuscular delivery of a single chain antibody gene reduces brain Abeta burden in a mouse model of Alzheimer’s disease. Neurobiol Aging. 2009;30(3):364–76. https://doi.org/10.1016/j.neurobiolaging.2007.06.013.

    Article  PubMed  CAS  Google Scholar 

  25. Yao XQ, Jiao SS, Saadipour K, Zeng F, Wang QH, Zhu C, et al. p75NTR ectodomain is a physiological neuroprotective molecule against amyloid-beta toxicity in the brain of Alzheimer’s disease. Mol Psychiatry. 2015;20(11):1301–10. https://doi.org/10.1038/mp.2015.49.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  26. Jiao SS, Yao XQ, Liu YH, Wang QH, Zeng F, Lu JJ, et al. Edaravone alleviates Alzheimer’s disease-type pathologies and cognitive deficits. Proc Natl Acad Sci U S A. 2015;112(16):5225–30. https://doi.org/10.1073/pnas.1422998112.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  27. Christakis DA, Ramirez JS, Ramirez JM. Overstimulation of newborn mice leads to behavioral differences and deficits in cognitive performance. Sci Rep. 2012;2:546. https://doi.org/10.1038/srep00546.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  28. Ruan CS, Yang CR, Li JY, Luo HY, Bobrovskaya L, Zhou XF. Mice with Sort1 deficiency display normal cognition but elevated anxiety-like behavior. Exp Neurol. 2016;281:99–108. https://doi.org/10.1016/j.expneurol.2016.04.015.

    Article  PubMed  CAS  Google Scholar 

  29. Zhang Q, Gao X, Li C, Feliciano C, Wang D, Zhou D, et al. Impaired dendritic development and memory in Sorbs2 knock-out mice. J Neurosci. 2016;36(7):2247–60. https://doi.org/10.1523/jneurosci.2528-15.2016.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  30. Bakoma B, Berke B, Eklu-Gadegbeku K, Agbonon A, Aklikokou K, Gbeassor M, et al. Acute and sub-chronic (28days) oral toxicity evaluation of hydroethanolic extract of Bridelia ferruginea Benth root bark in male rodent animals. Food Chem Toxicol. 2013;52:176–9. https://doi.org/10.1016/j.fct.2012.11.021.

    Article  PubMed  CAS  Google Scholar 

  31. Zhang Q, Li J, Zhang W, An Q, Wen J, Wang A, et al. Acute and sub-chronic toxicity studies of honokiol microemulsion. Regul Toxicol Pharmacol. 2014;71(3):428–36. https://doi.org/10.1016/j.yrtph.2014.11.007.

    Article  PubMed  CAS  Google Scholar 

  32. Wang L, Li Z, Li L, Li Y, Yu M, Zhou Y, et al. Acute and sub-chronic oral toxicity profiles of the aqueous extract of Cortex Dictamni in mice and rats. J Ethnopharmacol. 2014;158(Pt A):207–15. https://doi.org/10.1016/j.jep.2014.10.027.

    Article  PubMed  Google Scholar 

  33. Arjo G, Capell T, Matias-Guiu X, Zhu C, Christou P, Pinol C. Mice fed on a diet enriched with genetically engineered multivitamin corn show no sub-acute toxic effects and no sub-chronic toxicity. Plant Biotechnol J. 2012;10(9):1026–34. https://doi.org/10.1111/j.1467-7652.2012.00730.x.

    Article  PubMed  CAS  Google Scholar 

  34. West MJ. Regionally specific loss of neurons in the aging human hippocampus. Neurobiol Aging. 1993;14(4):287–93.

    Article  PubMed  CAS  Google Scholar 

  35. Arendash GW, King DL, Gordon MN, Morgan D, Hatcher JM, Hope CE, et al. Progressive, age-related behavioral impairments in transgenic mice carrying both mutant amyloid precursor protein and presenilin-1 transgenes. Brain Res. 2001;891:42–53.

    Article  PubMed  CAS  Google Scholar 

  36. Francis PT, Nordberg A, Arnold SE. A preclinical view of cholinesterase inhibitors in neuroprotection: do they provide more than symptomatic benefits in Alzheimer’s disease? Trends Pharmacol Sci. 2005;26(2):104–11. https://doi.org/10.1016/j.tips.2004.12.010.

    Article  PubMed  CAS  Google Scholar 

  37. Antunes M, Biala G. The novel object recognition memory: neurobiology, test procedure, and its modifications. Cogn Process. 2012;13(2):93–110. https://doi.org/10.1007/s10339-011-0430-z.

    Article  PubMed  CAS  Google Scholar 

  38. Hebert-Chatelain E, Desprez T, Serrat R, Bellocchio L, Soria-Gomez E, Busquets-Garcia A, et al. A cannabinoid link between mitochondria and memory. Nature. 2016;539(7630):555–9. https://doi.org/10.1038/nature20127.

    Article  PubMed  CAS  Google Scholar 

  39. Wolf A, Bauer B, Abner EL, Ashkenazy-Frolinger T, Hartz AM. A comprehensive behavioral test battery to assess learning and memory in 129S6/Tg2576 mice. PLoS One. 2016;11(1):e0147733. https://doi.org/10.1371/journal.pone.0147733.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  40. Vorhees CV, Williams MT. Morris water maze: procedures for assessing spatial and related forms of learning and memory. Nat Protoc. 2006;1(2):848–58. https://doi.org/10.1038/nprot.2006.116.

    Article  PubMed  PubMed Central  Google Scholar 

  41. Wang P, Su C, Li R, Wang H, Ren Y, Sun H, et al. Mechanisms and effects of curcumin on spatial learning and memory improvement in APPswe/PS1dE9 mice. J Neurosci Res. 2014;92(2):218–31. https://doi.org/10.1002/jnr.23322.

    Article  PubMed  CAS  Google Scholar 

  42. Tiwari SK, Agarwal S, Seth B, Yadav A, Nair S, Bhatnagar P, et al. Curcumin-loaded nanoparticles potently induce adult neurogenesis and reverse cognitive deficits in Alzheimer’s disease model via canonical Wnt/beta-catenin pathway. ACS Nano. 2014;8(1):76–103. https://doi.org/10.1021/nn405077y.

    Article  PubMed  CAS  Google Scholar 

  43. Kim DC, Ku SK, Bae JS. Anticoagulant activities of curcumin and its derivative. BMB Rep. 2012;45(4):221–6.

    Article  PubMed  CAS  Google Scholar 

  44. Takashi Ikeo IS. Age-related changes in hematology and serum biochemistry values in SAMR1 and SAMP8 mice. Shikaigaku. 2001;64(4):358–68. https://doi.org/10.18905/shikaigaku.64.4_358.

    Article  Google Scholar 

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Acknowledgments

Prof. Xin-Fu Zhou is grateful for the NHMRC fellowship. Ankit Parikh is obliged for the University President’s Scholarships from University of South Australia. Dr. Jintao Li is a visiting scholar and grateful for a scholarship under state scholarship fund organized by China Scholarship Council (CSC). We thank H. Md. Morshed Alam (BASF Australia Ltd.) for generously providing SOL, Rupal Pradhan and Andrew Beck from University of South Australia for technical support in hematological, coagulation parameters and histology study, Rebecca Summerton and Dr. Ian Beckman from Veterinary Diagnostic Laboratory, the University of Adelaide for providing technical support for serum biochemistry study, and Noralyn Manucat-Tan and Chun-Sheng Ruan for behavior tests. The Reid animal house staff members from University of South Australia are acknowledged for generous support in animal work.

Funding

This study received financial support from Fujian Kangshimei Co., China for the present research.

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Authors and Affiliations

Authors

Contributions

Sanjay Garg (SG) and Xin-Fu Zhou (XFZ) conceived the project. Ankit Parikh (AP), Krishna Kathawala (KK), Xia Cao (XC), XFZ, and SG designed the study. AP, KK, Chi Chen (CC), Jintao Li (JL), Zhengnan Shan (ZS), and XFZ performed the research. AP, KK, XFZ, and SG analyzed the data. AP, KK, XZ, and SG wrote the paper.

Corresponding authors

Correspondence to Xin-Fu Zhou or Sanjay Garg.

Ethics declarations

All breeding procedures were approved by the Animal Ethics Committee of the University of South Australia.

Conflict of interest

Ankit Parikh, Xin-Fu Zhou, and Sanjay Garg are the named inventors of Chinese patent 201610267974.5. Fujian Kangshimei Co., China owns the intellectual property. There is no other potential conflict of interest relevant to this article.

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Parikh, A., Kathawala, K., Li, J. et al. Curcumin-loaded self-nanomicellizing solid dispersion system: part II: in vivo safety and efficacy assessment against behavior deficit in Alzheimer disease. Drug Deliv. and Transl. Res. 8, 1406–1420 (2018). https://doi.org/10.1007/s13346-018-0570-0

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