Improved Biological Activity and Stability of enzyme L-Asparaginase in Solid Lipid Nanoparticles Formulation

Controlled release formulation of L-Asparaginase

Authors

  • Gazal Sharma PhD Researcher, IKG Punjab Technical University, Kapurthala, Punjab India
  • Goutam Rath Professor, Department of Pharmaceutics, ISF College of Pharmacy Moga, Punjab, India
  • Amit Goyal Scientist E, National Animal Institute of Biotechnology, Hyderabad, Andhra Pradesh India

Abstract

To protect the biological activity of an enzyme during the development of formulations is one of the biggest challenges. The tetrameric form of L-Asparaginase is used to treat Acute Lymphocytic Leukaemia. It possesses shorter in vivo half–life. Using a modified (water/oil)/water-emulsion method followed by solvent evaporation L-Asn was successfully encapsulated at the core of Solid Lipid Nanoparticles made of lipid glyceryl monostearate. This study elucidated that the preparation of L-Asn loaded SLN develop a colloidal formulation with enhanced activity. The in-vitro release profile of the enzyme revealed first bursts has been increased. The study of the lyophilised formulation also shows that the enzyme holds its biological activity and retains its particle size distribution. Consequently, by using an apt combination of homogenisation speed, temperature and additives the storage and biological activity of L-Asn in SLN formulation can be improved.

Keywords: L-Asparaginase, Solid Lipid Nanoparticles, Controlled release, Lymphocytic Leukaemia

DOI

https://doi.org/10.22270/jddt.v9i2-s.2708

Author Biographies

Gazal Sharma, PhD Researcher, IKG Punjab Technical University, Kapurthala, Punjab India

PhD Researcher, IKG Punjab Technical University, Kapurthala, Punjab India

Goutam Rath, Professor, Department of Pharmaceutics, ISF College of Pharmacy Moga, Punjab, India

Professor, Department of Pharmaceutics, ISF College of Pharmacy Moga, Punjab, India

Amit Goyal, Scientist E, National Animal Institute of Biotechnology, Hyderabad, Andhra Pradesh India

Scientist E, National Animal Institute of Biotechnology, Hyderabad, Andhra Pradesh India

References

Müller H.J., Boos J., Use of l-asparaginase in childhood ALL,. Critical. Review of Oncology, Haematology, 1998; 28:97–113

Cappizzi RL, Powell BL, Cooper MR, Stuart JJ, Muss HB, Richards F, Jackson DV et al, Sequential high-dose Ara-C and asparaginase in the therapy of previously treated and untreated patients with acute leukemia, Semin. Oncology 1985; 12:105–113.

Clarkson B, Krakoff Y, Burchenal J, Karnofsky D, Golbey R, Dowling M, Oettgen H, A. Lipton, Clinical results of treatment with E. coli L-asparaginase in adults with leukaemia, lymphoma, and solid tumors, Cancer, 1970; 25:279–305.

Cruz M.E.M., Gaspar M.M., Lopes F., Jorge J.S., Perez- Soler R., Liposomal L-Asparaginase: in vitro evaluation, International Journal of Pharmacy, 1993; 96:67–77.

Gaspar MM, Perez-Soler R, Cruz M.E.M., Biological characterization of L-asparaginase liposomal formulations, Cancer Chemotherapy and. Pharmacology, 1996; 38:373–377.

Neerunjun D, Gregoriadis G, Tumor regression with liposome-entrapped asparaginase: some immunological advantages, Biochemical Society Transactions, 1976; 4:133–134.

Ertl B., Gusenbauer C., Kudrnac M., Wirth M., Gabor F., Evaluation of the characteristics of protein-loaded poly(d,l-lactide-co-glycolide) nanospheres by preparation according to a central composite design. Scientia Pharmaceutica, 1999; 67, 289–304.

Wriston JC, Yellin TO, L-asparaginase, Advanced Enzymology, 1973; 39:185–248

Stecher A.L., de Deus P.M., Polikarpov, I., Abrahao-Neto, J., Stability of l-asparaginase: An enzyme used in leukaemia treatment, Pharmaceutica Acta Helvetiae, 1999; 74:1–9.

Sharif, S., O’Hagan, D.T., A comparison of alternative methods for the determination of the levels of proteins entrapped in poly(lactide-co-glycolide) microparticles. International Journal of Pharmaceutics, 1995; 115:259–263.

Gaspar M.M., Blanco D., Cruz M.E.M., Alonso M.J., Formulation of L-asparaginase-loaded PLGA Nanoparticles: Influence of polymer properties on enzyme loading, activity and in vitro release. Journal of Controlled Release, 1998; 52:53–62.

Diwan M., Park T.G., PEGylation enhances protein stability during encapsulation in PLGA microspheres. Journal of Controlled Release 2001; 73:233–244.

Published

2019-04-15
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How to Cite

1.
Sharma G, Rath G, Goyal A. Improved Biological Activity and Stability of enzyme L-Asparaginase in Solid Lipid Nanoparticles Formulation: Controlled release formulation of L-Asparaginase. J. Drug Delivery Ther. [Internet]. 2019 Apr. 15 [cited 2026 Feb. 1];9(2-s):325-9. Available from: https://www.jddtonline.info/index.php/jddt/article/view/2708

How to Cite

1.
Sharma G, Rath G, Goyal A. Improved Biological Activity and Stability of enzyme L-Asparaginase in Solid Lipid Nanoparticles Formulation: Controlled release formulation of L-Asparaginase. J. Drug Delivery Ther. [Internet]. 2019 Apr. 15 [cited 2026 Feb. 1];9(2-s):325-9. Available from: https://www.jddtonline.info/index.php/jddt/article/view/2708