Formulation and Characterization of Solid Self- Microemulsifying Cefuroxime Axetil Products

DOI:

https://doi.org/10.37285/ijpsn.2014.7.3.9

Authors

  • Satish Puttachari
  • Navanath V. Kalyane
  • Sarbani Duttagupta
  • Koushik Yetukuri

Abstract

The Cefuroxime axetil has been used in treatment of wide range of infections but exhibits poor and variable bioavailability thus it is difficult to establish optimal oral dosage schedule. The purpose of this work was to prepare stable solid self-microemusifying drug delivery system (S-SMEDDS) of cefuroxime to improve the solubility and dissolution. The saturation solubility of drug in oils, solvents, surfactants and co-surfactants were determined and ternary phase diagram was drawn. Based on the results SMEDDS were prepared and characterized for self-emulsification properties and in-vitro dissolution. One of the best SMEDDS formulations was converted to S-SMEDDS by adsorption technique using maltodextrin as adsorbent. SEM of the S-SMEDDS revealed that particles were well separated and were free flowing, characterization by DSC, XRD revealed no interaction between drug and excipients. In-vitro dissolution was rapid and complete and no marked changes in physical and emulsification property were observed on stability. 

Downloads

Download data is not yet available.

Metrics

Metrics Loading ...

Keywords:

Self-emulsification, Adsorption technique, Scanning electron microscope

Downloads

Published

2014-08-31

How to Cite

1.
Puttachari S, Kalyane NV, Duttagupta S, Yetukuri K. Formulation and Characterization of Solid Self- Microemulsifying Cefuroxime Axetil Products. Scopus Indexed [Internet]. 2014 Aug. 31 [cited 2024 Nov. 19];7(3):2567-73. Available from: https://ijpsnonline.com/index.php/ijpsn/article/view/739

Issue

Section

Research Articles

References

Ajay kumar, Surabhi Sharma, Ravindrakamble (2010). Self emulsifying drug delivery system (SEDDS): future aspects. Int J Pharm Sci 2(4): 7-13.

Ajay U. Kyatanwar (2010). Solid self-emulsifying drug delivery system (SEDDS): future aspects. J Pharm Res 2: 7-13.

Anna Szlagowska, MichaKaza, Piotr J. Rudzki (2010). Validated HPLC method for determination of cefuroxime in human plasma. ActaPoloniaePharmaceutica - Drug Res 67(6): 677-681.

Arora SC, Sharma PK, Irchhaiya R, Khatkar A, Singh N, Gagoria J (2010). Development, characterization and solubility study of solid dispersions of cefuroxime axetil by the solvent vaporation method. J Adv Pharm Tech Res. 1: 326-329

Bo Tang, Gang Cheng, Jian-Chun Gu (2008). Development of solid self-emulsifying drug delivery systems: preparation techniques and dosage forms. Drug Discovery Today 13: 606-612.

Bhagwat DA, D’Souza John I (2012). Development of Solid Self Micro Emulsifying Drug Delivery System with Neusilin US2 for Enhanced Dissolution Rate of Telmisartan. Int J Drug Dev& Res. 4(4): 398-407.

Gudigennavar AS, Vijapur LS, Patil CC, Kulkarni RV (2013). Development and evaluation of gastro-retentive drug delivery systems of cefuroxime Axetil. Afr J PharmPharmacol. 7(20): 1332-1338.

Jannin V, Musakhanian J, Marchaud D (2008). Approaches for the development of solid and semi-solidm lipid-based formulations. Adv. Drug Deliv Rev 60: 734-46.

Karunakar Reddy T (2011). Recent trends in Development of Solid-self emulsifying drug delivery (S-SEDDS) Systems: An overview. Res J Pharm Sci Biotech 1: 1-5.

Koushik Y, Preethi S, Satish P, Uma Shankar MS, Thakur RS (2013). Development of Solid-Self Micron Emulsifying Drug Delivery Systems. Int J Pharm SciNanotech 6(2): 6-16.

Nekkanti V, Karatgi P, Prabhu R, Pillai R (2010). Solid self-microemulsifying formulation for candesartan cilexetil. AAPS Pharm Sci Tech 11(1): 9-17.

Prabagar Balakrishnan, Beom-Jin Lee b, Dong Hoon Oh et al., (2009). Enhanced oral bioavailability of dexibuprofen by a novel solid Self-emulsifying drug delivery system (SEDDS). Enhanced oral bioavailability of dexibuprofen by a novel solid Self-emulsifying drug delivery system (SEDDS). Eur J Pharma and Biopharma 72: 539–545.

Ravindra SD, Shailesh VB, SuyogAher, Anant R. Paradkar (2009).Cefuroxime axetilsolid dispersion with polyglycolized glycerides forimproved stability andbioavailability. JPharmPharmacol 6:743-751.

Ruiz-Carretero PM, Merino-Sanjuan, Nácher A, Casabo VG (2004). Pharmacokinetic models for the saturable absorption of cefuroxime axetil and saturable elimination of cefuroxime. Eur J Pharm Sci. 21: 217-223.

SatishPuttachari, Koushik Yetkuri, Shrinivas Pachava (2013). Solid-Self emulsifying drug delivery system an alternative to SEDDS.UniJPharm 2(3): 38-46.

SatishPuttachari, Navanath. VK, SarbaniDuttagupta (2013). Design and Evaluation of Self-Micro Emulsifying Drug Delivery Systems (SMEDDS) of CefuroximeAxetil.IntJPharmSci Rev Res.22(1): 70-74

Srinivasan S, Baskaran R, Balakrishnan P, Pritam T, Chul Soon Yong et al., (2011). Solidself-nanoemulsifying drug delivery system (S-SNEDDS) containing phosphatidylcholine for enhanced bioavailability of highly lipophilic bioactive carotenoid lutein. Eur J PharmBiopharm. 79(2): 250-27.

Suman Katteboina (2009). Approaches for the development of solid self-emulsifying drug delivery systems and dosage forms. Asian J Pharm Sci. 4: 240-253.

The United States of Pharmacopoeia (2011): 34th revision and National Formulary 29th Asian edition; Vol II. The United States of Pharmacopoeial convention, Rockville.

Wonkyung Cho, Min-Soo Kim, Jeong-Soo Kim, Junsung Park, Hee Jun Park et al., (2013). Optimized formulation of solid self-microemulsifying sirolimus delivery systems. IntJNanomedicine. 8: 1673-1682.