Spherically agglomerated solid dispersions of valsartan to improve solubility, dissolution rate and micromeritic properties

Authors

  • Amit R. Tapas Sudhakarrao Naik Institute of Pharmacy, Pusad-445204, Yavatmal, Maharashtra, India
  • Pravin S. Kawtikwar Shri Sureshdada Jain Institute of Pharmaceutical Education and Research, Jamner-424206, Jalgaon, Maharashtra, India
  • Dinesh M. Sakarkar Shri Sureshdada Jain Institute of Pharmaceutical Education and Research, Jamner-424206, Jalgaon, Maharashtra, India.

Keywords:

Valsartan, Spherical agglomeration, Solid dispersion, Solubility, Dissolution rate, Micromeritic properties

Abstract

The objective of the present work was to enhance the solubility and dissolution rate of valsartan (VAL) a poorly water soluble antihypertensive, by spherically agglomerated solid dispersions using methanol, water and dichloromethane as good solvent, poor solvent and bridging liquid, respectively. The hydrophilic polymers like polyvinyl pyrrolidone, Hydroxypropyl β-cyclodextrin, Hydroxypropyl methylcellulose were used in agglomeration process. The pure drug (VAL) and its agglomerates with different polymers were characterize by differential scanning calorimetry (DSC), X-ray diffraction (XRD), IR spectroscopic studies and scanning electron microscopy (SEM). The DSC results indicated that decrease in melting enthalpy related to disorder in the crystalline content. XRD studies also showed changes in crystallanity, IR spectroscopy revealed that there were no chemical changes in the recrystallized agglomerates. The spherically agglomerated solid dispersions with different polymers exhibited marked increase in solubility, dissolution rate and micromeritic properties (bulk density, flow property, compactability) compared with VAL. The SEM studies showed that the agglomerates posseeses a good spherical shape.

References

Dhirendra K, Lewis

dispersions: a review. Pak J Pharm Sci 2009; 22:

-246.

Vasconcelos T, Sarmento B, Costa P. Solid

dispersion as strategy to improve oral

bioavailability of poor water soluble drugs. Drug

Disc Toady 2007; 12: 1068-1075.

Sharma DK, Joshi SB. Solubility enhancement

strategies for poorly water-soluble drugs in solid

dispersions: a review. Asian J Pharm 2007; 1: 9-

Gupta VR, Mutalik S, Patel MM, Jani GK.

Spherical crystals of celecoxib to improve

solubility, dissolution rate and micromeritic

properties. Acta Pharm 2007; 57: 173-184.

Usha AN, Mutalik S, Reddy MS, Rajith AK,

Kushtagi P, Udupa N. Preparation and, in vitro,

preclinical

spherical agglomerates. Eur J Pharm Biopharm

; 70: 674-683.

Yadav AV, Yadav VB. Designing of

pharmaceuticals to improve physicochemical

properties by spherical crystallization technique, J

Pharm Res 2008; 1: 105-112.

Kawashima Y, Cui F, Takeuchi H, Niwa T, Hino

T, Kiuchi K. Improvements in flowability and

compressibility of pharmaceutical crystals for

direct tabletting by spherical crystallization with a

two solvent system, Powder Technol 1994; 78:

-157.

Bodmeier R, Paeratakul R. Spherical

agglomerates of water-insoluble drugs, J Pharm

Sci 1989; 78: 964-967.

Di Martino P, Barthelemy C, Piva F, Joiris E,

Palmieri GF, Martelli S. Improved dissolution

behavior of fenbufen by spherical crystallization,

Drug Dev Ind Pharm 1999; 25: 1073-1081.

Sano A, Kuriki T, Kawashima Y, Takeuchi H,

Hino T, Niwa T. Par

spherical crystallization technique. V.

Improvement of dissolution and bioavailability of

direct compressed tablets prepared using

tolbutamide agglomerated cry m 1

Bull 1992; 40: 3030-3035.

Cui F, Yang M, Jiang Y, Cun D, Lin W, Fan Y,

Kawashima Y. Design of sustained-release

nitrendipine microspheres having solid dispersion

structure by quasi-emulsion solvent diffusion

method, J

Kawashima Y. Development of spherical

crystallization technique and its application to

pharmaceutical system,

-151.

Hu R, Zhu J, Chen G, Sun Y, Mei K, Li S.

Preparation of sustained-release simvastatin

microspheres by the spherical crystalliz

technique, Asian J Pharm Sci 2006; 1: 47-52.

Yang M, Cui F, You B, Fan Y, Wang L, Yue P,

Yang H. Preparation of sustained-release

nitrendipine microspheres with Eudragit RS and

Aerosil using quasi-emulsion solvent diffusion

method, Int J Pharm 2003; 259: 103-113.

Criscione L, Gasparo M

Whitebread S, Ramjoue HP, Wood JM.

Pharmacological profile of valsartan: a potent,

orally active, nonpeptide antagonist of the

angiotensin II AT1-receptor subtype, Br J

Pharmacol 1993; 110: 761-771.

Dina R, Jafari M. Angiotensin II receptor

antagonists: an overview, Am J Health Syst

Pharm 2000; 57: 1231-1241.

Lobenberg

bioavailability, bioequivalence and

biopharmaceutics classification system: new

scientific approaches to international regulatory

standards. Eur J Pharm Biopharm 2000; 50: 3-12.

Brunella C, Clelia DM, Ma

Improvement of solubility and stability of

valsartan by hydroxypropyl-beta-cyclodextrin. J

Incl Phenom Macrocycl Chem

Wells J. Pharmaceutical preformulation, the

physicochemical properties of drug substances.

In: M.E. Aulton (ed.), Pharmaceutics- the science

of dosage form design. 2nd ed. Churchill Livingst

M

In

pL2SooDU

methods for drug products Website. Available at:

http://www.accessdata.fda.gov/scripts/cder/dissol

ution/dsp_SearchResultsDissolutions.cfm?PrintAl

l=1. Accessed November 7, 2009.

Khan KA. The concept of dissolution efficiency.

J. Pharm Pharmacol 1975; 27:48-49.

Anderson NH, Bauer M, Boussac N, Khan-Malek

R, Munden P, Sardaro M. An evaluation of fit

factors and dissolution efficiency for the

comparison of in vitro dissoluti

Pharm Biomed Anal 1998; 17:811–822.

Huang HH, Huang C. Preparation of solid

coprecipitates of amorphous valsartan, US Patent

US 20070166372A1, 2007.

Rukhman I, Flyaks

Polymorphs of valsartan. US Patent US

B2,

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Published

2010-12-31

How to Cite

Amit R. Tapas, Pravin S. Kawtikwar, & Dinesh M. Sakarkar. (2010). Spherically agglomerated solid dispersions of valsartan to improve solubility, dissolution rate and micromeritic properties. International Journal of Drug Delivery, 2(4), 304–313. Retrieved from https://ijdd.arjournals.org/index.php/ijdd/article/view/43

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Original Research Articles