Formulation And Development Of Nanocrystals By Using Natural Amino Acid

Authors

  • Bhujbal N S
  • Karthickeyan K

Keywords:

Nanocrystals, Bovine Serum Albumin, Desolvation

Abstract

Objective: The primary target of this study was to formulate and invitro study of BSA loaded nanocrystal containing paclitaxel as a novel method by desolvation technique. The impact of various test on the particle size, entrapment efficiency, percent drug released etc. was assessed. The 32 full factorial designs was employed to investigate the influence of formulation variables on nanocrystals characteristics.

Method: BSA loaded nanocrystals were prepared by using desolvation technique. Nanocrystals were prepared by using BSA and PVP K 30; these were characterized for various methods such as shape, size and, entrapment efficiency and Zeta Potential, Drug excipients compatibility which is determined by FTIR.

Result: FTIR shows there was no interaction between formulation ingredients. The average particle size was found251.3 nm. The size of nanoparticles increases with BSA-PVP polymer concentration. Prepared nanocrystal shows drug content 96.04% and Entrapment Efficiency 92.05% with particle size 251.3 nm. In-vitro drug releases shows maximum 96.07%.

Conclusion: By using desolvation method BSA loaded nanocrystals was successfully prepared and evaluated, containing good particle size, EE% and zeta potential % drug release so by doing further in vivo study it could be good choice for conventional drug delivery system

Downloads

Download data is not yet available.

References

Jahanshahi, M., Zhang, Z., & Lyddiatt, A. Subtractive chromatography for purification and recovery of Nano-Bioproducts. IEE Proceedings – Nanobiotechnology 2009; 152(3): 121.

. Soppimath, K. S., Aminabhavi, T. M., Kulkarni, A. R., & Rudzinski, W. E.. Biodegradable polymeric nanoparticles as drug delivery devices. Journal of Controlled Release 2001; 70(1-2): 1–20.

.Van Eerdenbrugh, B., Vermant, J., Martens, J. A., Froyen, L., Humbeeck, J. V., Van den Mooter, G., & Augustijns, P. Solubility increases associated with crystalline drug nanoparticles: Methodologies and significance. Molecular Pharmaceutics 2010; 7(5): 1858–1870.

.Rabinow, B. E. Nanosuspensions in drug delivery. Nature Reviews Drug Discovery2004; 3(9): 785–796.

. Abdelbary, A. A., Li, X., El-Nabarawi, M., Elassasy, A., & Jasti, B. Effect of fixed aqueous layer thickness of polymeric stabilizers on zeta potential and stability of Aripiprazole nanosuspensions. Pharmaceutical Development and Technology2012; 18(3): 730–735.

MÖSchwitzer, J., Nadiem Bushrab, F., & MÜLler, R.. Manufacturing of nanoparticles by milling and homogenization techniques. Drugs and the Pharmaceutical Sciences. 2006;

. Ali, H. S. M., York, P., & Blagden, N. Preparation of hydrocortisone nanosuspension through a bottom-up nanoprecipitation technique using microfluidic reactors. International Journal of Pharmaceutics 2009; 375(1-2):107–113.

. Van Eerdenbrugh, B., Vermant, J., Martens, J. A., Froyen, L., Van Humbeeck, J., Augustijns, P., & Van den Mooter, G. A screening study of surface stabilization during the production of drug nanocrystals. Journal of Pharmaceutical Sciences 2009; 98(6): 2091–2103.

. Kreuter, J. Colloidal drug delivery systems;2014

Tian, J., Liu, J., Tian, X., Hu, Z., & Chen, X. Study of the interaction of Kaempferol with bovine serum albumin. Journal of Molecular Structure 2004; 691(1-3): 197–202.

. Trnkova, L., Bousova, I., Kubicek, V., & Drsata, J. Binding of naturally occurring hydroxycinnamic acids to bovine serum albumin. Natural Science 2010; 02(06):563–570.

. Xu, H., Yao, N., Xu, H., Wang, T., Li, G., & Li, Z. Characterization of the interaction between Eupatorin and bovine serum albumin by spectroscopic and Molecular Modeling Methods. International Journal of Molecular Sciences 2013; 14(7):14185–14203.

. Javadzadeh, Y., Musaalrezaei, L., & Nokhodchi, A. Liquisolid technique as a new approach to sustain propranolol hydrochloride release from tablet matrices. International Journal of Pharmaceutics 2008; 362(1-2):102–108.

. Surini, S., & Prakoso, K. Preparation and characterization of chitosan succinate as coating polymer for enteric-coated tablet. International Journal of Applied Pharmaceutics 2018; 10(1):343.

. Aburahma, M. H., & Abdelbary, G. A. Novel diphenyl dimethyl bicarboxylate provesicular powders with enhanced hepatocurative activity: Preparation, optimization, in vitro/in vivo evaluation. International Journal of Pharmaceutics 2012; 422(1-2):139–150.

. Xu, H., He, L., Nie, S., Guan, J., Zhang, X., Yang, X., & Pan, W. Optimized preparation of vinpocetine proliposomes by a novel method and in vivo evaluation of its pharmacokinetics in New Zealand rabbits. Journal of Controlled Release 2009; 140(1): 61–68.

. Elhissi, A., Hidayat, K., Phoenix, D. A., Mwesigwa, E., Crean, S. J., Ahmed, W., Faheem, A., & Taylor, K. M. G. Air-jet and vibrating-mesh nebulization of NIOSOMES generated using a particulate-based proniosome technology. International Journal of Pharmaceutics 2013; 444(1-2):193–199.

Soliman, S. M., Abdelmalak, N. S., El-Gazayerly, O. N., & Abdelaziz, N. Novel non-ionic surfactant proniosomes for transdermal delivery of lacidipine: Optimization using 23factorial design andin vivoevaluation in Rabbits. Drug Delivery 2016; 23(5):1608–1622.

Downloads

Published

2025-07-10

How to Cite

1.
N S B, K K. Formulation And Development Of Nanocrystals By Using Natural Amino Acid. J Neonatal Surg [Internet]. 2025Jul.10 [cited 2025Oct.10];14(32S):4757-65. Available from: https://www.jneonatalsurg.com/index.php/jns/article/view/8194