Literature DB >> 14621964

Preparation and characterization of novel coenzyme Q10 nanoparticles engineered from microemulsion precursors.

Cheng-Hsuan Hsu1, Zhengrong Cui, Russell J Mumper, Michael Jay.   

Abstract

The purpose of these studies was to prepare and characterize nanoparticles into which Coenzyme Q10 (CoQ10) had been incorporated (CoQ10-NPs) using a simple and potentially scalable method. CoQ10-NPs were prepared by cooling warm microemulsion precursors composed of emulsifying wax, CoQ10, Brij 78, and/or Tween 20. The nanoparticles were lyophilized, and the stability of CoQ10-NPs in both lyophilized form and aqueous suspension was monitored over 7 days. The release of CoQ10 from the nanoparticles was investigated at 37 degrees C. Finally, an in vitro study of the uptake of CoQ10-NPs by mouse macrophage, J774A.1, was completed. The incorporation efficiency of CoQ10 was approximately 74% +/- 5%. Differential Scanning Calorimetry (DSC) showed that the nanoparticle was not a physical mixture of its individual components. The size of the nanoparticles increased over time if stored in aqueous suspension. However, enhanced stability was observed when the nanoparticles were stored at 4 degrees C. Storage in lyophilized form demonstrated the highest stability. The in vitro release profile of CoQ10 from the nanoparticles showed an initial period of rapid release in the first 9 hours followed by a period of slower and extended release. The uptake of CoQ10-NPs by the J774A.1 cells was over 4-fold higher than that of the CoQ10-free nanoparticles (P < .05). In conclusion, CoQ10-NPs with potential application for oral CoQ10 delivery were engineered readily from microemulsion precursors.

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Year:  2003        PMID: 14621964      PMCID: PMC2750625          DOI: 10.1208/pt040332

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  26 in total

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2.  Self-emulsifying drug delivery systems (SEDDS) of coenzyme Q10: formulation development and bioavailability assessment.

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3.  Analysis of ubidecarenone (CoQ10) aqueous samples using reversed phase liquid chromatography.

Authors:  S Nazzal; A A Zaghloul; I K Reddy; M A Khan
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5.  Positively charged nanoparticles for improving the oral bioavailability of cyclosporin-A.

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Authors:  Zhengrong Cui; Cheng-Hsuan Hsu; Russell J Mumper
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  11 in total

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3.  Polymer particle shape independently influences binding and internalization by macrophages.

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5.  The cytotoxic effects of lipidic formulated gold porphyrin nanoparticles for the treatment of neuroblastoma.

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Review 6.  PLA micro- and nano-particles.

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7.  Innovative coenzyme Q10-loaded nanoformulation as an adjunct approach for the management of moderate periodontitis: preparation, evaluation, and clinical study.

Authors:  Mohamed A Shaheen; Samah H Elmeadawy; Fagr B Bazeed; Mohamed M Anees; Noha M Saleh
Journal:  Drug Deliv Transl Res       Date:  2020-04       Impact factor: 4.617

8.  A comparative evaluation of coenzyme Q10-loaded liposomes and solid lipid nanoparticles as dermal antioxidant carriers.

Authors:  Evren H Gokce; Emrah Korkmaz; Sakine Tuncay-Tanrıverdi; Eleonora Dellera; Giuseppina Sandri; M Cristina Bonferoni; Ozgen Ozer
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9.  Development of biodegradable nanoparticles for oral delivery of ellagic acid and evaluation of their antioxidant efficacy against cyclosporine A-induced nephrotoxicity in rats.

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10.  Effects of In Ovo Injection of Coenzyme Q10 on Hatchability, Subsequent Performance, and Immunity of Broiler Chickens.

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