ABSTRACT:
Objective: Nanotechnology enhances the solubility, bioavailability and the rate of solubility of drugs whose solubility of water is very weak. The primary goals of creating nanocrystals are to enhance the bioavailability of weakly soluble drugs, streamline the administration of Metaxalone (MTX) via the all routes and enhance solubility and pharmacokinetic performance. Material and Methods: The solvent diffusion approach was utilized to create drug nanocrystals without surfactants by employing stabilizers such cyclodextrin (CD). A cooling centrifuge was utilized to perform high-speed centrifugation in order to separate the nanocrystal from the nanosuspension. Differential scanning calorimetry (DSC), electron microscopy (SEM), FTIR analysis, powder X-ray diffraction analysis, solubility analysis, Particle size range and zeta potential measurement, in-vitro dissolution and ex-vivo permeation study were used to evaluate and characterized the results. Results: MTX nanocrystal formulation 8 (MNC 8) has better solubility than MNC 7. The nanocrystal was created in MNC 7, MNC 8, and MNC 9, according to the z-average values 448 to 11850nm and zeta potential value for MNC 8 and MNC 7 was found -8.62±3.99 and -10.4±9.13. FTIR spectrum of MNC 8, characteristic peaks that were seen at 3441, 1733, 1082, 3602, 2922, 1641 and 2354 cm-1. In its crystal state, MNC 8 diffraction angles were determined to be 5.01, 10.25, 13.34, 14.18, 17.87, 19.03 and 22.40º. The endothermic peak of DSC at 124ºC confirms the observed melting point of MTX, which is 121ºC. According to DSC thermograms, the melting point range was 120-125ºC. Drugs demonstrated 11% membrane penetration at 1 hour, but MTX permeability through MTX nanocrystals was 15-17%. Better MTX nanocrystal solubility was confirmed at 6 hours with a 46% drug release in MTX solution and a 58-65% drug release in the formulation. MNC 8 exhibited a higher drug content than MNC 7 and MNC 9 among the formulations. Conclusion: Franz diffusion cell apparatus used a biological membrane (egg cell membrane) to conduct an ex-vivo drug release research of MTX and MTX nanocrystal. Compared to pure MTX, formulated MTX nanocrystal exhibits superior drug release.
Cite this article:
Nadir Khan, Saurabh Srivastava. Metaxalone-cyclodextrin Loaded Starch Nanocrystal Based Formulation Design, Development and Control Release Evaluation. Research Journal Pharmacy and Technology. 2026;19(3):1282-8. doi: 10.52711/0974-360X.2026.00183
Cite(Electronic):
Nadir Khan, Saurabh Srivastava. Metaxalone-cyclodextrin Loaded Starch Nanocrystal Based Formulation Design, Development and Control Release Evaluation. Research Journal Pharmacy and Technology. 2026;19(3):1282-8. doi: 10.52711/0974-360X.2026.00183 Available on: https://www.rjptonline.org/AbstractView.aspx?PID=2026-19-3-44