An overview on cubic liquid crystalline nanoparticles-trig lipid drug delivery system

Authors

  • M. Dharani Department of Pharmaceutics, Vignan Pharmacy College,Vadlamudi, Guntur, Andhra Pradesh, India
  • K. Rama Devi Department of Pharmaceutical Analysis, Vignan Pharmacy College,Vadlamudi, Guntur, Andhra Pradesh, India.

DOI:

https://doi.org/10.47957/ijpda.v12i2.595

Keywords:

Cubosomes, Nanoparticles, Bicontinuous, Carvenous (honeycomb), Pharmaceutical division

Abstract

This type of complex structure allows them greater drug loading ability, because of increased surface area and cuboidal structures, they have simple method of preparation and have ability to encapsulate hydrophilic, hydrophobic and amphiphilic substances. Cubosomes increases the solubility of poorly soluble drugs. Cubosomal dispersions are bioadhesive and biocompatible in nature. These are versatile systems, administered by different ways such as oral, perctuneous and parental routes. Cubosomes have broad vast applications in many areas and are characterized by various parameters consequently cubosomes are in move forward of awareness by pharmaceutical development division. Cubosomes, sometimes referred to as bicontinuous cubic phase liquid crystals, are spherical, quadruple nanoparticles with an interior cubic lattice mostly composed of certain amphiphilic lipids in a particular proportion. Cubosomes often arise when a solid-like phase is dispersed into smaller particles after a surfactant or polar lipid is hydrated to form a cubic phase. With distinct qualities of practical interest, they exhibit solid like rheology. They are thermodynamically stable, self-assembling drug delivery devices. Water and lipid bicontinuous domains give cubosomes their carvenous structure. Three-dimensional bilayers are formed by tightly twisted honeycomb arrangements.

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Published

2024-06-30
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How to Cite

M, D., and R. D. K. “An Overview on Cubic Liquid Crystalline Nanoparticles-Trig Lipid Drug Delivery System ”. International Journal of Pharmaceutics and Drug Analysis, vol. 12, no. 2, June 2024, pp. 8-13, doi:10.47957/ijpda.v12i2.595.

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