4.7 Article

Development and in vivo/in vitro evaluation of novel herpetrione nanosuspension

Journal

INTERNATIONAL JOURNAL OF PHARMACEUTICS
Volume 441, Issue 1-2, Pages 227-233

Publisher

ELSEVIER
DOI: 10.1016/j.ijpharm.2012.11.039

Keywords

Herpetrione; Nanosuspension; Dissolution; Bioavailability; Activity assay

Funding

  1. Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry [20101561]
  2. Natural Science Found of Beijing city of China [7122176]
  3. National Natural Science Foundation of China [81102821]
  4. Natural Science Found of Jiangxi Province [20122BAB215038]

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Herpetrione (HPE), is a new compound extracted from Herpetospermum caudigerum, which is proved to be a novel and potent antiviral agent. However, due to poor water solubility, oral bioavailability of the drug was relatively low. To improve the dissolution and absorption of the drug, formulation of HPE as nanosuspension has been performed in this study. HPE nanosuspension were produced by high pressure homogenization and transformed into dry powder by lyophilization. The nanosuspension was then investigated using photon correlation spectroscopy (PCS), zeta potential measurement, SEM and PXRD. To verify the theoretical hypothesis on the benefit of decreased particle size and increased surface area, in vitro dissolution characterization and in vivo pharmacokinetics were investigated. The inhibitory effect on HBsAg, HBeAg, and HBV-DNA of HPE nanosuspension in 2.2.15 cells was studied. Results showed that a narrow size distributed nanosuspension with a mean particle size of 286 +/- 1.3 nm, a polydispersity index of 0.18 +/- 0.06 and a zeta potential of -26.9 +/- 2.4 mV was obtained. The result of PXRD showed that HPE was amorphous state in both coarse powder and nanosuspension. In the in vitro dissolution test, HPE nanosuspension showed an increased dissolution velocity markedly. In the in vivo evaluation, compared to coarse HPE, nanosuspension exhibited significant increase in AUC(0-t), C-max and decrease in T-max, MRT. The inhibitory effect of HBsAg, HBeAg, and HBV-DNA of 2.2.15 cells treated by HPE nanosuspension were stronger than those of the HPE. The in vitro activity experiments provided evidence for an enhanced efficacy of the HPE nanosuspension formulation compared to HPE coarse suspension. These results revealed that particle size reduction could enhance HPE dissolution rate and absorption in gastrointestinal tract, and nanosuspension might be a good choice for oral delivery of poor bioavailability drug like HPE. (C) 2012 Elsevier B. V. All rights reserved.

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