INFLUENCE OF HYDROPHILIC POLYMERS ON COMPLEXATION AND SOLUBLIZING EFFICIENCIES OF BETA CYCLODEXTRIN OVER SILYMARIN

Similar documents
EFFECT OF PVP ON CYCLODEXTRIN COMPLEXATION OF EFAVIRENZ FOR ENHANCING ITS SOLUBILITY AND DISSOLUTION RATE

Investigations of polyethylene glycol mediated ternary molecular inclusion complexes of silymarin with beta cyclodextrins

ENHANCEMENT OF SOLUBILITY AND DISSOLUTION RATE OF NIMESULIDE BY CYCLODEXTRINS, POLOXAMER AND PVP

A FACTORIAL STUDY ON ENHANCEMENT OF SOLUBILITY AND DISSOLUTION RATE OF IBUPROFEN BY β CYCLODEXTRIN AND SOLUTOL HS15

Chemate and Chowdary, IJPSR, 2012; Vol. 3(7): ISSN:

FACTORIAL STUDIES ON THE EFFECTS OF HYDROXY PROPYL β- CYCLODEXTRIN AND POLOXAMER 407 ON THE SOLUBILITY AND DISSOLUTION RATE OF BCS CLASS II DRUGS

Available online at

The Effect of Water Soluble Polymers on Felodipine Aqueous Solubility and Complexing Abilities with Natural and Modified β-cyclodextrin

ENHANCEMENT OF SOLUBILITY, DISSOLUTION RATE AND BIOAVAILABILITY OF RITONAVIR BY CYCLODEXTRINS AND SOLUTOL HS15 - A FACTORIAL STUDY

A FACTORIAL STUDY ON THE ENHANCEMENT OF DISSOLUTION RATE OF KETOPROFEN BY SOLID DISPERSION IN COMBINED CARRIERS

FORMULATION AND EVALUATION OF VALSARTAN TABLETS EMPLOYING CYCLODEXTRIN-POLOXAMER 407-PVP K30 INCLUSION COMPLEXES

International Journal of Research in Pharmaceutical and Nano Sciences Journal homepage:

FORMULATION AND EVALUATION OF ETORICOXIB TABLETS EMPLOYING CYCLODEXTRIN- POLOXAMER PVPK30 INCLUSION COMPLEXES

Scholars Research Library. Formulation Development of Pioglitazone Tablets Employing β Cyclodextrin- Poloxamer 407- PVP K30: A Factorial Study

CHAPTER VI FACTORIAL STUDIES ON THE EFFECTS OF CYCLODEXTRINS AND SOLUTOL HS15 ON THE SOLUBILITY AND DISSOLUTION RATE OF EFAVIRENZ AND RITONAVIR

Research Article. Nanosuspension versus cyclodextrin inclusion of ciprofloxacin for solubility and dissolution enhancement

A FACTORIAL STUDY ON THE ENHANCEMENT OF DISSOLUTION RATE OF ACECLOFENAC BY SOLID DISPERSION IN STARCH PHOSPHATE AND GELUCIRE

Int. Res J Pharm. App Sci., 2012; 2(6): ISSN:

FORMULATION AND CHARACTERIZATION OF TELMISATAN SOLID DISPERSIONS

K. Ravi Shankar et al. /BioMedRx 2013,1(3), Available online through

Asian Journal of Pharmacy and Life Science ISSN Vol. 1 (4), Oct-Dec, 2011

Int. Res J Pharm. App Sci., 2013; 3(6):42-46 ISSN:

Optimization of valsartan tablet formulation by 2 3 factorial design

Int. Res J Pharm. App Sci., 2013; 3(4): ISSN:

Available online at

Synergistic Effect of PEG-400 and Cyclodextrin to Enhance Solubility of Progesterone Submitted: November 20, 2002; Accepted: January 9, 2003

ENHANCEMENT OF SOLUBILITY OF BICALUTAMIDE DRUG USING SOLID DISPERSION TECHNIQUE

Research Article Derivative Spectrophotometric Method for Estimation of Metformin Hydrochloride in Bulk Drug and Dosage Form

STUDIES ON EFFECT OF BINDERS ON ETORICOXIB TABLET FORMULATIONS

Ansari, IJPSR, 2016; Vol. 7(3): E-ISSN: ; P-ISSN:

SOLID INCLUSION COMPLEXES OF CLASS II IMIDAZOLE DERIVATIVE WITH Β CYCLODEXTRIN. Pradesh.

Development and validation of spectrophotometric method for simultaneous estimation of Sumatriptan and Naproxen sodium in tablet dosage form

Journal of Pharmaceutical and Scientific Innovation

A STUDY ON SUITABILITY OF NIMESULIDE-BETACYCLODEXTRIN COMPLEX IN ORAL AND TOPICAL DOSAGE FORMS

Journal of Chemical and Pharmaceutical Research, 2018, 10(2): Research Article

ISSN: X CODEN: IJPTFI Available Online through Research Article

Development and Validation of a New Uv Method for the Analysis of Rebamipide

A Comparative Evaluation of Cross Linked Starch Urea-A New Polymer and Other Known Polymers for Controlled Release of Diclofenac

SOLUBILITY AND STABILITY ENHANCEMENT OF CURCUMIN THROUGH CYCLODEXTRIN COMPLEXATION

Comparative Dissolution Study of Glipizide by Solid Dispersion Technique

IJRPC 2011, 1(4) Rohan et al. ISSN: INTERNATIONAL JOURNAL OF RESEARCH IN PHARMACY AND CHEMISTRY

Development and validation of UV spectrophotometric estimation of lisinopril dihydrate in bulk and tablet dosage form using area under curve method

skim milk as carrier by kneading method. They were evaluated for percentage yield, drug content, FT-IR

International Journal of Pharma and Bio Sciences

Formulation and Evaluation of Tinidazole Syrup Made by Mixed Solvency Concept Technique

0 9 : >?! 0 (.56± E

Patel B et al. IRJP 1 (1)

MEDAK DIST. ANDHRA PRADESH STATE, INDIA. Research Article RECEIVED ON ACCEPTED ON

Journal of Chemical and Pharmaceutical Research, 2018, 10(1): Research Article

EFFECT OF STARCH HYDROLYSATES IN THE PROCESS OF DISSOLUTION OF SOLIDS

DEVELOPMENT OF UV SPECTROPHOTOMETRIC METHOD FOR THE ESTIMATION OF EZETIMIBE FROM TABLET FORMULATION

Available Online through Research Article

pharmaceutical formulations. Anagliptin shows absorption maximum at 246 nm and obeys beer s law in the

Journal of Chemical and Pharmaceutical Research

Asian Journal of Pharmacy and Life Science ISSN Vol. 2 (2), July-Sept,2012

Preparation and Evaluation of Ethyl Cellulose Coated Microcapsules of Carbamazepine for Controlled Release

PHARMA SCIENCE MONITOR AN INTERNATIONAL JOURNAL OF PHARMACEUTICAL SCIENCES

Mixed Hydrotropy: Novel Science of Solubility Enhancement

PREPARATION, CHARACTERIZATON AND DISSOLUTION KINETICS OF CELECOXIB : β AND HP β -CYCLODEXTRIN COMPLEXES

J Pharm Sci Bioscientific Res (4): ISSN NO

Reverse Phase HPLC Analysis of Atomoxetine in Pharmaceutical Dosage Forms

210 J App Pharm Vol. 6; Issue 2: ; April, 2014 Mustafa et al, 2014

Asian Journal of Pharmaceutical Analysis and Medicinal Chemistry Journal home page:

ASSAY AND IMPURITY METHOD FOR DURACOR TABLETS BY HPLC

Quantitative estimation of Rosuvastatin in bulk and tablet dosage form by using area under curve method

Development, Estimation and Validation of Lisinopril in Bulk and its Pharmaceutical Formulation by HPLC Method

Evaluation of Ethyl Cellulose as Microencapsulating Agent for Controlled Release of Glimepiride

Development and validation of analytical methods for estimation of imatinib mesylate in bulk and solid dosage forms by UV spectroscopy

Scholars Research Library

Journal of Chemical and Pharmaceutical Research, 2013, 5(1): Research Article

>>> Oral Formulation Optimization. Introduction. A Tiered Approach for Identifying Enabling Formulations

Research Article. ISSN Available online at 746

DESIGN AND EVALUATION OF CONTROLLED RELEASE MATRIX TABLETS OF FLURBIPROFEN

DEVELOPMENT AND VALIDATION OF RP-HPLC METHOD FOR QUANTITATIVE ANALYSIS TOLBUTAMIDE IN PURE AND PHARMACEUTICAL FORMULATIONS

DEVELOPMENT AND VALIDATION OF COLORIMETRIC METHODS FOR THE DETERMINATION OF RITONAVIR IN TABLETS

Spectrophotometric method development and validation for estimation of Tizanidine and Aceclofenac in Bulk Drug & Tablet formulation

Validated Spectrophotometric Method for Simultaneous Estimation of Atorvastatin and Nicotinic acid in Combined Pharmaceutical dosage form

Formulation Development of Aceclofenac Tablets Employing Starch Phosphate -A New Modified Starch

The present manuscript describes simple, sensitive, rapid, accurate, precise and cost effective First derivative

International Journal of Advances in Pharmacy and Biotechnology Vol.3, Issue-1, 2017, 1-7 Research Article Open Access.

Preparation and Evaluation of Silymarin Controlled Release Tablets Prepared Using Natural Gums

Method Development and Validation of Emtricitabine in Bulk by UV Spectroscopy

International Journal of Pharma Sciences and Scientific Research

Development and Validation of UV- Spectrophotometric Method for Estimation of Simvastatin in Bulk and Solid Dosage Form.

IJPAR Vol.3 Issue 4 Oct-Dec-2014 Journal Home page:

ISSN (Print)

Available Online through Research Article

Characterization and Solubility Studies of Mefloquinehydrochloride Inclusion Complexes with α - Cyclodextrin/ Hydroxypropyl α -Cyclodextrin.

Enhancement of flavonols water solubility by cyclodextrin inclusion complex formation - case study

Journal of Advanced Scientific Research. Formulation and Evaluation of Glimepiride Solid Dispersion Tablets for Their Solubility Enhancement

DEVELOPMENT AND EVALUATION OF ORAL RECONSTITUTABLE SYSTEMS OF CEPHALEXIN

First Order Derivative Spectrophotometric Method for Estimation of Melatonin in Bulk and Pharmaceutical Dosage Form

Validated RP-HPLC Method for the Estimation of Esomeprazole Enteric Coated Tablets

FORMULATION AND EVALUATION OF PIROXICAM AND CELECOXIB TABLETS EMPLOYING PROSOLVE BY DIRECT COMPRESSION METHOD

Available online Research Article

Preparation and Evaluation of Ethylene Vinyl Acetate Copolymer Coated Microcapsules of Glipizide for Controlled Release

Department Of Quality Assurance Techniques, Modern College of Pharmacy Nigdi, Pune Maharashtra, India

DEVELOPMENT OF RP-HPLC METHOD FOR ESTIMATION OF DROTAVERINE HYDROCHLORIDE IN PHARMACEUTICAL FORMULATIONS

DEVELOPMENT AND VALIDATION OF SPECTROPHOTOMETRIC METHOD FOR DETERMINATION OF METOPROLOL SUCCINATE

Development and validation of UV and RP-HPLC method for estimation of Nepafenac in bulk drug and opthalmic formulation

Transcription:

: 2414-2423 ISSN: 2277 4998 INFLUENCE OF HYDROPHILIC POLYMERS ON COMPLEXATION AND SOLUBLIZING EFFICIENCIES OF BETA CYCLODEXTRIN OVER SILYMARIN ANSARI MJ 1*, AHMED MM 1, FATIMA F 1, ANWER MK 1, JAMIL S 1, AL-SHDEFAT R 1, ALI BE 1, AL AWMI F 1 AND ABDEL-KADER MS 2 1: Department of Pharmaceutics, College of Pharmacy, Salman Bin Abdul Aziz University, Al- Kharj, Saudi Arabia 2: Department of Pharmacognosy, College of Pharmacy, Salman Bin Abdul Aziz University, Al- Kharj, Saudi Arabia *Corresponding Author: E Mail: javedpharma@gmail.com; Contact No. +96615886041; Fax: +96615886001 ABSTRACT Silymarin exhibits very low bioavailability (23 47%) due to its poor aqueous solubility and hence it needs improvement in the solubility and dissolution rate so as to enhance bioavailability and to derive its maximum therapeutic efficacy. Though cyclodextrin complexation and use of water-soluble polymers for enhancing the solubility of silymarin have been investigated separately, no reports are available on their combined use in enhancing the solubility. The objective of the present investigation is to study the complexation of silymarin with β- cyclodextrin alone and in the presence of hydrophilic polymers by phase solubility study and to evaluate the feasibility of enhancing the solubility of silymarin. The aqueous solubility of silymarin was linearly increased as a function of the concentration of β-cyclodextrin alone and in the presence of hydrophilic polymers, PVP, HPMC and PEG 6000. The increase in solubility was due to the formation of a 1: 1 M complexes in solutions. The complexes formed between β- cyclodextrin and silymarin were quite stable as indicated by apparent stability constants. Addition of hydrophilic polymers has markedly enhanced the complexation efficiency of β- cyclodextrin. Of the investigated polymers, PVP has given the highest enhancement in the 2414

complexation efficiency of β-cyclodextrin. The order of hydrophilic polymers in enhancing the complexation efficiency was PVP > HPMC > PEG 6000. Hydrophilic polymers have markedly enhanced the solubilizing efficiency of β-cyclodextrin. PVP has given highest enhancement (12.67 fold) in the solublizing efficiency of β-cyclodextrin. Hence, a combination of β- cyclodextrin and hydrophilic polymers is recommended for enhancing solubility of silymarin. Keywords: Silymarin, Cyclodextrin Complexation, Hydrophilic Polymers, Ternary Phase Solubility INTRODUCTION β-cyclodextrin (BCD) is the most widely used of water-solublepolymer to aqueous CD host molecule for inclusion complexes solution has been shown to improve affecting physical and chemical properties, like solubility and stability of several guest complexation efficiency of CDs [5-8]. The aim of this work was to examine whether molecules [1]. It comprises the most widely water-soluble polymers improve used pharmaceutical excipient to enhance solubility of several water insoluble or poorly soluble drugs in recent years due to low cost and their approval by various regulatory complexation efficiency of BCD for silymarin (SLM), a poorly water-soluble drug with significant hepato-protective activity [9]. It is a mixture of three flavanolignans, namely, agencies [2, 3]. Unfortunately, the silybin, silydianin, and silicristine, with complexation efficiency of BCD is rather low and consequently a significant amount of silybin being most active [10]. Due to poor water solubility its bioavailability is as low as BCD is required to make inclusion 23 47% [11]. Although cyclodextrin complexes. Moreover, commonly used complexation [11] and use of water-soluble excipients in drug formulation may further polymers for enhancing the solubility and reduce complexation efficiency thus dissolution rate of silymarin have been necessitating excessive use of BCD [4], which investigated individually [12-14], no report is increases formulation bulk making it available on their combined use in enhancing unsuitable for oral administration especially of low potency herbal drugs. Thus, it is necessary to develop methods that can be the solubility and dissolution rate. In the present study the individual and combined effect of BCD and water-soluble polymers on applied to enhance the complexation the solubility of SLM were investigated. efficiency of BCD. Addition of small amount 2415

MATERIALS AND METHODS Chemicals Beta cyclodextrin (β-cd), Poly vinyl pyrrolidone K30 (PVP), PEG 6000 and HPMC 4000 cps were purchased from Sigma Aldrich Chemical Co. USA. Silymarin was purchased from Loba chemie Banglore, India. All other solvents and chemicals were of analytical grade and obtained from Sigma- Aldrich, USA. Standard Plot of Silymarin 10 mg of standard Silymarin was accurately weighed, dissolved in methanol and diluted with distilled water (DW) to get a concentration of about100 µg/ml. From this solution, suitable aliquots were transferred into 10 ml volumetric flask and diluted with DW to get concentrations 1, 2, 4, 6, 8, and 10, µg/ml of SLM which were then analyzed by double beam UV spectrophotometer (Model V-630 Jasco, Japan) at 286 nm. Phase Solubility Studies Solubility studies (with BCD and hydrophilic polymers separately and in combinations) were performed according to the method reported by Higuchi and Connors [15]. Excess amount of SLM was incubated at 25 C and 100 RPM in biological shaker with 0-20 mm of BCD solutions or hydrophilic polymers (0-2% w/v) or BCD 0-20 mm containing 0.5% w/v of hydrophilic polymers. Suspensions were filtered using 0.45 micron membrane filter after 72 hours and amount of SLM in solutions were analyzed by double beam UV spectrophotometer (Model V-630 Jasco, Japan) after appropriate dilution. To nullify the absorbance due to the presence of CD and polymers, the apparatus were calibrated with the corresponding blank in every measurement. The apparent stability constants (Kc) were estimated from the straight line of the phase solubility diagrams according to the equation of Higuchi and Connors. RESULTS The influence of BCD concentration in the presence or absence of water-soluble polymer on the solubility of SLM was studied using the method of Higuchi and Connors. This is based on monitoring changes in the solubility of a SLM by the addition of BCD or polymers or both in combinations. The Phase solubility diagram of SLM in aqueous βcd and polymer solutions were shown in Figure 1 and Figure 2 respectively. Both demonstrated A L type equilibrium phase solubility diagram as SLM solubility increases linearly as a function of BCD and polymer concentrations. The phase-solubility studies diagrams obtained with BCD alone and in presence of water-soluble polymers is shown in Figure 3. 2416

They displayed A L type equilibrium phase solubility diagrams for SLM: BCD binary and ternary systems, showing that SLM solubility increase linearly as a function of BCD concentration and that the soluble complexes were formed without occurrence of precipitation in the range of BCD concentration used. The slope values were found to be less than one suggesting the formation of 1:1 stoichiometry complexes in solution and allowing to the calculation of the apparent stability constants (Kc) of the SLM: BCD complexes as per the Higuchi and Connors equation. The apparent stability constant (Kc) in each case was calculated from the slope of the corresponding linear plot of the phase solubility diagram according to the equation, Kc = Slope/So (1-Slope), where So is the solubility of the drug in the absence of solublizers (BCD or hydrophilic polymers). The estimated Kc values of various complexes are given in Table 1. To evaluate the effect of polymers on the solublizing efficiency of BCD, the solublizing efficiency was calculated in each case as the ratio between drug solubility in aqueous solution of BCD (20 mm with or without hydrophilic polymers) and in water. The solublizing efficiency values are given in Table 2. BCD alone gave a 6.79 fold increase in the solubility of SLM, whereas 7.09, 9.12 and 12.77 fold increase was observed in the presence of PEG 6000, HPMC and PVP respectively. Thus the addition of polymers has markedly enhanced the solublizing efficiency of BCD. Table 1: Apparent Stability Constants of Various SLM: BCD complex systems with and without polymers Solvents Kc (M -1 ) *Complexation efficiency BCD 286.074 - BCD + PEG 6000 337.812 1.18 BCD+ HPMC 492.281 1.72 BCD +PVP 881.138 3.08 *(No of folds of increase in Kc): Ratio between Kc of BCD with and without polymers 2417

Solubility of SLM (µg.ml -1 ) Ansari MJ et al Table 2: Solubility of SLM in water, aqueous solutions of polymers (0.5 % W/V), aqueous solutions of BCD (20 mm), and ternary mixtures (0.5 % W/V polymers + 20 mm BCD) Solvents Solubility of SLM(µg.ml -1 ) *Solubilizing efficiency Water 377 - BCD 2562 6.79 PEG 6000 639 1.69 BCD + PEG 6000 2675 7.09 HPMC 1017 2.70 HPMC + BCD 3444 9.12 PVP 1307 3.46 PVP + BCD 4821 12.77 *Ratio between drug solubility in aqueous solutions (BCD 20 mm with OR without hydrophilic polymers) and in water. 3000 2500 2000 1500 1000 500 0 0 1 2 4 8 16 20 Conc. of βcd (mm.ml -1 ) Figure 1: Phase solubility diagram of SLM in BCD 2418

Solubility of Silymarine (mm) Solubility of SLM (µg.ml -1 ) Ansari MJ et al 2500 2000 PVP HPMC PEG 6000 1500 1000 500 0 0 0.25 0.5 0.75 1 1.5 2 Polymer % (w/v) Figure 2: Phase Solubility Diagram of SLM in Different Polymer Solutions 0.0120 BCD BCD:HPMC BCD-PEG BCD:PVP 0.0100 y = 0.408x + 0.001 0.0080 y = 0.278x + 0.001 0.0060 y = 0.209x + 0.001 0.0040 y = 0.183x + 0.001 0.0020 0.0000 0.000 0.002 0.004 0.006 0.008 0.010 0.012 0.014 0.016 0.018 0.020 Concentration of BCD (mm) Figure 3: Phase solubility diagram of SLM in binary and ternary mixtures 2419

Solubility of SLM (µg.ml -1 ) Ansari MJ et al BCD PEG 6000-BCD HPMC-BCD PVP-BCD 6000 5000 4000 3000 2000 1000 0 0 1 2 4 8 16 20 Conc. of βcd (mm.ml -1 ) Figure 4: Phase Solubility Diagrams of SLM: BCD with or without polymers DISCUSSION It has been observed that addition of watersoluble polymers to the BCD solution did not change the type of phase-solubility diagrams obtained for binary systems and resulted in increase in stability constant (Figure 3). The observed enhancement of stability constant with addition of the polymers shows that all investigated polymers were able to interact with SLM-BCD binary complexes. The solublizing effect of CDs was increased in the presence of 0.5% (W/V) polymers in following order PVP> HPMC >PEG 6000, consequently, a synergistic effect in SLM solubility was observed in the presence of these polymers Table 2 and Figure 4. Water- soluble polymers increase the solublizing effect of cyclodextrin by increasing Kc of the drug-cd complexes, as reported by several authors [5, 16]. This increase enhances the complexation efficiency and thus less cyclodextrin is needed for solublizing a given amount of drug when hydrophilic polymers are present in the aqueous media. In the present work addition of small amount of polymers to cyclodextrin solutions resulted in higher Ks values for ternary complexes in comparison to corresponding binary ones suggesting a significant improvement in the complexation efficiency between SLM-BCD thereby markedly enhancing the solublizing 2420

efficiency of BCD and this is in agreement with previous reports [17-19]. CONCLUSION The complexation of SLM with BCD was investigated by phase solubility studies. The phase solubility diagrams for the complex formation between SLM and BCD in the presence and absence of hydrophilic were evaluated. The aqueous solubility of SLM was increased linearly as a function of the concentration of BCD. The phase solubility diagrams of SLM-BCD complexes can be classified as type A L according to Higuchi and Connors. Because the straight line had a slope < 1 in each case, the increase in solubility was due to the formation of a 1: 1 M complex in solution with BCD both; in the presence and absence of hydrophilic polymers. The values of Kc indicated that all the complexes formed between SLM and BCDare quite stable. The values of stability constant (Kc) were found to be higher in the presence of hydrophilic polymers indicating higher complexation efficiency. We observed a 2.33, 1.93 and 1.26 fold increase in the Kc values, in the presence of PVP, HPMC and PEG 6000 respectively. PVP has given higher enhancement in complexation efficiency. The order of hydrophilic polymers in enhancing the complexation efficiency was PVP > HPMC >PEG 6000. ACKNOWLEDGEMENTS Authors are grateful to Dean, College of Pharmacy, for providing opportunity, resourses, instrumentation and facility to carryout and complete this research project. REFERENCES [1] Fromming KH and Szejtli J: in K.H. Frömming and J. Szejtli (eds.), Cyclodextrins Inclusion Complexes (Cyclodextrin in Pharmacy), Vol.5, Kluwer Academic Publishers, Dordrecht, 1994, pp. 45 81. [2] Thomson Do, Cyclodextrins--enabling excipients: their present and future use in pharmaceuticals, Crit Rev Ther. Drug Carries Syst. 1997, 14(1), 1-104. [3] Hedges AR, Industrial Applications of Cyclodextrins, Chem. Rev., 1998, 98(5), 2035-2044. [4] Loftsson T, Másson M and Sigurjonsdottir JF, Methods to enhance the complexation efficiency of cyclodextrins S.T.P., Pharma Sci., 1999, 9(3), 237-242. [5] Loftsson T, Increasing the cyclodextrin complexation of drugs and drug bioavailability through addition of water-soluble polymers, Pharmazie, 1998, 53 (11), 733-740. [6] Mura P, Faucci MT and Bettinetti GP, The influence of polyvinylpyrrolidone 2421

on naproxen complexation with hydroxypropyl-beta-cyclodextrin, Eur J. Pharm. Sci., 2001, 13(2), 187-194. [7] Koester LS, Mayorga P and BassaniVL,.Carbamazepine/betaCD/H PMC solid dispersions. I. Influence of the spray-drying process and betacd/hpmc on the drug dissolution profile, Drug Dev. Ind. Pharm., 2003, 29(2), 139-144. [8] Chowdary KPR and Madhavi BLR, Novel drug delivery technologies for insoluble drugs, Indian Drugs, 2005, 42 (9), 557. [9] Abrol S, Trehan A, Katare OP. Comparative study of different silymarinformulations: formulation, characterisation and in vitro/in vivo evaluation, Curr. Drug. Deliv., 2005, 2(1), 45-51. [10] Kvasnicka F, Biba B, Sevcik R, Voldrich M and Kratka J, Analysis of the active components of silymarin, J. Chromatogr. A., 2003, 990 (1-2), 239-245. [11] Ghosh A, Biswas S, Ghosh T, Preparation and Evaluation of Silymarin β-cyclodextrin Molecular Inclusion Complexes, J. Young Pharm., 2011, 3(3), 205-210. [12] Li FQ, Hu JH, Improvement of the dissolution rate of silymarin by means of solid dispersions, Chem. Pharm. Bull., 2004, 52(8), 972-973. [13] Qiu MF, Jia W, Li SS, Xu ZH, Sun X, Wang XR, Zhang YY, Xie GX, A new silymarin preparation based on solid dispersion technique, Adv. Ther., 2005, 22(6), 595-600. [14] Hwang DH, Kim YI, Cho KH, Poudel BK, Choi JY, Kim DW, Shin YJ, Bae ON, Yousaf AM, Yong CS, Kim JO, Choi HG, A novel solid dispersion system for natural productloaded medicine: silymarin-loaded solid dispersion with enhanced oral bioavailability and hepato-protective activity, J. Microencapsul., 2014,25 In press. [15] Higuchi T and Connors KA, In C.N. Reill (ed.), Phase-Solubility Techniques (Advances in Analytical Chemistry and Instrumentation, Wiley-Inter sciences, New York, 1965, pp. 117 212. [16] Savolainen J, Jarvinen K, Taipale H, Jarho P, Loftsson T and Jarvinen T, Co-administration of a water-soluble polymer increases the usefulness of cyclodextrins in solid oral dosage 2422

forms, Pharma Res., 1998, 15(11), 1696-1701. [17] Fridriksdottir H, Loftsson T, Gudmundsson JA, Bjarnason GJ, Kjeld M and Thorsteinsson T, Design and in vivo testing of 17 betaestradiol-hp beta CD sublingual tablets, Pharmazie, 1996, 51 (1), 39-42. [18] Fridriksdottir H, Loftsson T and Stefansson E, Formulation and testing of methazolamide/cyclodextrin eye drop solutions, J. Contl. Rel., 1997, 44, 95-99. [19] Cappello B, Carmignani C, Iervolino M, La RotondaMI and Saettone MF, Solubilization of tropicamide by hydroxypropyl-beta-cyclodextrin and water-soluble polymers: in vitro/in vivo studies, Int. J. Pharm., 2001, 213 (1-2), 75-81. 2423