Author(s):
Patil MD, Keny RV, Pimprikar RB, Yashwante SB, Saindane DS, Mandlik SK, Mujawar Tabrej, Kale MK, Firke BM
Email(s):
manoj16885@yahoo.co.in
DOI:
Not Available
Address:
Patil MD*1, Keny RV1, Pimprikar RB2, Yashwante SB2, Saindane DS2 , Mandlik SK1, Mujawar Tabrej2, Kale MK3 and Firke BM3
1 Government College of Pharmacy, Goa
2 Gangamai College of Pharmacy, Nagaon, Dhule(M.S.)
3 KYDSCT’s College of Pharmacy, Sakegaon, Tal. Bhusawal, Dist. Jalgaon (M.S.)
*Corresponding Author
Published In:
Volume - 1,
Issue - 3,
Year - 2009
ABSTRACT:
The effect of molecular weight of polyethylene glycols (PEGS) and drug/PEG ratio on the structure and dissolution rates of the solid dispersions with Telmisartan have been examined. Telmisartan (TEL) was chosen as a model drug due to its poor and pH dependent water solubility. The alkalizer used to modify the pH of TEL was NaOH, in the SD system significantly increased the drug dissolution rate in gastric fluid (pH 1.2) . Structural change in drug crystallinity to an amorphous form was also a contributing factor based on differential scanning calorimetry (DSC) thermograms and powder X-ray diffraction (PXRD) patterns. The drug frequency of the C=O band decreased and the O–H broad band in the Fourier transform infrared (FTIR) spectra disappeared when this alkalizer was added. It was evident that the alkalizer in PEG 6000 based SDs synergistically enhanced dissolution of TEL not only by modulating pH but also by changing drug crystallinity to an amorphous form via molecular interactions.
Cite this article:
Patil MD, Keny RV, Pimprikar RB, Yashwante SB, Saindane DS , Mandlik SK, Mujawar Tabrej, Kale MK, Firke BM. Physicochemical Characterization of Solid Dispersion of Telmisartan with Alkaliser by Hot Melt Method. Research J. Pharma. Dosage Forms and Tech. 2009; 1(3):250-253 .
Cite(Electronic):
Patil MD, Keny RV, Pimprikar RB, Yashwante SB, Saindane DS , Mandlik SK, Mujawar Tabrej, Kale MK, Firke BM. Physicochemical Characterization of Solid Dispersion of Telmisartan with Alkaliser by Hot Melt Method. Research J. Pharma. Dosage Forms and Tech. 2009; 1(3):250-253 . Available on: https://rjpdft.com/AbstractView.aspx?PID=2009-1-3-19