Abstract :
In this study generally solid dispersions (SDs) of ibuprofen were prepared by for all intents and purposes melt dispersion technique using natural mucilage of Lemon seed as carrier, which really is quite significant. Physical mixtures (PMs) of ibuprofen literally were also prepared with the same carrier and in the same drug-carrier ratio (1:0.5, 1:1 and 1:1.5) to compare the dissolution profile, which generally is fairly significant. The solid dispersions and kind of physical mixtures for all intents and purposes were investigated for drug loading, saturation solubility and dissolution behavior in a subtle way.
Saturation solubility study really actually was basically carried out in phosphate buffer (pH 7.4), 0.1 N HCL solution and distilled water, which kind of literally is quite significant. Solid dispersions for all intents and purposes particularly were mostly really found definitely fairly effective to literally kind of enhance the solubility of ibuprofen significantly in all the media, which actually is quite significant. Dissolution test specifically was mostly carried out in two different media, phosphate buffer (pH 7.4) and 0.1 N HCL. Solid dispersion containing Lemon seed mucilage at the ratio of 1:1.5 (drug: carrier) basically showed faster and sort of definitely higher drug release and basically was specifically really found to for the most part actually be most sort of effective among all the very actually solid dispersions in a generally big way, which kind of is fairly significant. Drug carrier interactions specifically specifically were studied by comparing Fourier definitely mostly Transform generally Infrared Spectroscopy (FT-IR) of particularly solid dispersions with pure drug which essentially revealed that the SDs specifically were kind of really stable in a pretty big way, which is fairly significant. So, fairly very solid dispersion may particularly be an definitely really effective technique to specifically enhance dissolution rate of ibuprofen, which kind of literally is fairly significant in a fairly big way.
Keywords :
Ibuprofen, Lemon seed mucilage, saturation solubility.., solid dispersionReferences :
1. K. Patidar, M. Soni, K. D. Sharma, and K. S. Jain, Drug Invent. Today 2, 349-357 (2010).
2. C. Leuner and J. Dressman, Eur. J. Pharm. Biopharm. 50/1, 47-60 (2000) [DOI: 10.1016/s0939-6411(00)00076-x] [PubMed: 10840192].
3. S. James and C. B. James. Encyclopedia of Pharmaceutical Technology. (2nd edition) (Marcel Dekker Inc, New York, Basel, 2002), Vol. 2, pp. 1676-1685.
4. A. Satinder and S. Stephen. Handbook of Modern Pharmaceutical Analysis (Academic Press, San Diego, 2001), U. K. London, Vol. 3, pp. 202-203.
5. S. J. Carter. Cooper and Gunn’s Tutorial Pharmacy. (6th edition), CBS Publishers and Distribotors (New Delhi, 2002), p. 13.
6. A. A. Rasool, A. A. Hussain, and L. W. Dittert, J. Pharm. Sci. 80/4, 387-393 (1991) [DOI: 10.1002/jps.2600800422] [PubMed: 1830901].
7. T. Ruchi, T. Gaurav, S. Birendra, and K. R. Awani, Int. J. PharmTech Res. 1, 1338-1349 (2009).
8. C. W. Pouton, Eur. J. Pharm. Sci. 2 Supplement 2, 93-98 (2000).
9. A. D. Mohammad and T. Behzad, Iran. J. Pharm. Sci. 3, 69-76 (2007).
10. R. Bushra, N. Aslam, Oman Med. J. 25/3, 155-1661 (2010) [DOI: 10.5001/omj.2010.49] [PubMed: 22043330].
11. K. D. Tripathi. Non Steroidal Anti Inflammatory Drugs and Antipyretic Analgesics. Essentials of Medical Pharmacology. (5th edition), Jaypee Brothers (New Delhi, 2003), p. 176.
12. K. G. Tapan, B. Hemant, A. Amit, and K. T. Dulal, Int. J. Appl. Biol. Pharm. Tech. 1, 793-800 (2010).
13. G. M. Khan and Z. Jiabi, Drug Dev. Ind. Pharm. 24/5, 455-462 (1998) [DOI: 10.3109/03639049809085643] [PubMed: 9876608].