Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Application of Mathematical Models in Drug Release Kinetics of Lagerstroemia Speciosa Extract-phospholipid Complex


Affiliations
1 Associate Professor, Sal Institute of Pharmacy, Opp. Science City, Ahmedabad 380061, Gujarat,, India
2 NIMS Institute of Pharmacy, Jaipur, Rajasthan,, India
3 Anand Pharmacy College, Gujarat,, India
     

   Subscribe/Renew Journal


The aim of present work is to govern and scrutinize the kinetics of drug release from the complex by employing various mathematical models. A study was done with Lagerstroemia speciosa extract-phospholipid complex, 50 mg/200mg by employing anticipation precipitation technique using soya lecithin and cholesterol as complex forming polymer. In-vitro drug release profile was carried out in phosphate buffer saline, pH 7.4 (900mL) using USP dissolution apparatus II (Paddle) at 50 RPM at an extended time period of 0.5, 0.75, 1, 1.5, 2, 2.5, 3 and 4 hours. The drug release data was obtained, quantitatively correlated and interpreted with various mathematical models viz. Zero order model, first order model, Higuchi model and Korsmeyer-Peppas model and evaluated to understand the kinetics of drug release. The criterion for the most suitable model was based on the high degree of coefficient of correlation of drug release profile was best fitted with Korsmeyer-Peppas model and follows drug release kinetics which is diffusion controlled.

Keywords

Lagerstroemia speciosa extract-phospholipid complex; Diffusion; Coefficient of correlation; Kinetics of drug release.
Subscription Login to verify subscription
User
Notifications
Font Size


  • James E Polli. In-Vitro studies are sometimes better than conventional human pharmacokinetic in vivo studies in assessing bioequivalence of immediate-release solid oral dosage forms. AAPS, 2008; 10:289-99.
  • Mistry Khushboo, Kavya Naik, Vasanthi, Alicia Menezes, Anup Naha, K.B. Koteshwara, K. Girish Pai. Formulation and Evaluation of Irbesartan nanosuspension for Dissolution Enhancement. Research J. Pharm. and Tech. 2017; 10(9): 3043-3048.
  • Paulo Costa, Jose Manuel Sousa Lobo. Modeling and comparison of dissolution profiles. Eur J Pharm Sci 2001; 13:123-33
  • Thakkar VT, Shah PA, et al. Goodness-of-fit model-dependent approach for release kinetics of levofloxacin hemihydrates floating tablet. Dissolution Technologies. 2009; 16: 35-39.
  • Dash S, Murthy PN, Nath L, Chowdhury P. Kinetic modeling on drug release from controlled drug delivery systems. Acta Pol Pharm, 2010; 67: 217-223.
  • Subal CB. Modelling of Drug release: The Higuchi equation and its application. 2006, Pharmabiz.com.
  • Singhvi G, Singh M. In-vitro drug release characterization models. Int J Pharm Stud Res.2011; 2: 77-84.
  • Ittadwar PA, Puranik PK. Novel Umbelliferone Phytosomes: Development and Optimization Using Experimental Design Approach and Evaluation Of Photo- Protective And Antioxidant Activity. International Journal of Pharmacy and Pharmaceutical Sciences. 2017; 9(1):218-228.
  • KalitaB, Das MK, Sharma AK. Novel phytosome formulations in making herbal extracts more effective. Research Journal of Pharmaceutical Technology. 2013; 6:1295-301.
  • Shende M, Kolhe DB, Jaiswal NM. Herbosomes: herbo-phospholipid complex an approach for absorption enhancement. International Journal of Biological and Pharmaceutical Research. 2012; 3:946-55.
  • ChoubeyA. Phytosome–a novel approach for herbal drug delivery. International Journal of Pharmaceutical Science Research. 2011; 2:807-815.
  • Brack SD. Controlled Drug Delivery,vols.1 and 2,CRCPress,Oxford,1984.
  • Herman J, Remon JP. Modified starches as hydrophilic matrices for controlled oral delivery, In vitro drug release evaluation of thermally modified starches. International Journal of Pharmaceutics. 1989; 56:65-70.
  • Patel Anar J. A Systematic review on Banaba. International Journal of research and analytical reviews. 2020; 7(1): 608-616.
  • ChoubeyA. Phytosome–a novel approach for herbal drug delivery. International Journal of Pharmaceutical Science Research. 2011; 2:807-815.
  • Brack SD. Controlled Drug Delivery,vols.1 and 2,CRCPress,Oxford,1984.
  • Parmar NS and ShivprakashN. Controlled and Novel Drug Delivery, CBS Publisher, New Delhi, 1997.
  • Deepak Karki, Gururaj S. Kulkarni, Shivakumar Swamy, Sheeba FR. Formulation and Evaluation of Mucoadhesive Buccal Tablets of Curcumin and its Bioavailability Study. Research J. Pharm. and Tech 2017; 10(12): 4121-4128.
  • Pawan Singh, Prevesh Kumar, Neelkant Prasad. Formulation and Evaluation of Aspirin Tablets by Using Different Lubricants in Combination for better Kinetic Drug Release Study by PCP. Research J. Pharm. and Tech. 2017; 10(9): 2934-2938.
  • S. B. Gondkar, Neha R. Patil, R. B. Saudagar. Formulation Development and Characterization of Etodolac Loaded Transethosomes for Transdermal Delivery. Research J. Pharm. and Tech. 2017; 10(9): 3049-3057.
  • Welling PG. A Review of Development of Controlled Release Delivery Systems. Drug Development. 1983; 9:1185-1195.
  • Shende M, Kolhe DB, Jaiswal NM. Herbosomes: herbo-phospholipid complex an approach for absorption enhancement. International Journal of Biological and Pharmaceutical Research. 2012; 3:946-55.
  • ChoubeyA. Phytosome–a novel approach for herbal drug delivery. International Journal of Pharmaceutical Science Research. 2011; 2:807-815.
  • Brack SD. Controlled Drug Delivery,vols.1 and 2,CRCPress,Oxford,1984.
  • Parmar NS and ShivprakashN. Controlled and Novel Drug Delivery, CBS Publisher, New Delhi, 1997.
  • N. Raghavendra Babu, Y. Padmavathi, S. Priyanka, P. Ravi Kumar. Development of Sensitive Spectrophotometric Method for Analysis of Darifenacin Hydrobromide Liposomes in Rat Plasma. Asian J. Pharm. Ana. 2017; 7(1): 41-47.
  • Karthick J., Praveen Kumar P.K., SujathaLoganathan P.L. In-Silico Analysis of Targeted Drug Delivery to Hepatic Cells using Lipid Nano-Particles to Treat Liver Diseases. Asian J. Pharm. Tech. 2013; Vol. 3: Issue 4, Pg 189-194.
  • Dattatraya M. Shinkar, Pinak S. Paralkar, R.B. Saudagar. An Overview on Trends and Developments in Liposome – as Drug Delivery System. Asian J. Pharm. Tech. 2015; Vol. 5(4) : 231-237.
  • Aditya Singh, Ansari VA, Md. Faheem Haider, Juber Akhtar, Farogh Ahsan. Essential oils used in Modified Drug Delivery and its formulation of Liposomes for Topical Purpose. Res. J. Pharmacology and Pharmacodynamics.2020; 12(1):34-38.
  • Derle D.V., Kasliwal N.H., Gandhi P.P., Yeole D.R. Development, Characterization and Evaluation of Niosomes and Liposomes of Bacitracin Zinc. Research J. Pharm. and Tech; Oct.-Dec.2010; 3 (4): 1295-1300.
  • Banker GS, Siepmann J, Rhodes C. Modern pharmaceutics. CRC Press, Florida, USA, 2002.
  • Rescigno A. Foundation of Pharmacokinetics. University of Minnesota, Kluwer Academic/ Plenum Publishers, New York, USA, 2003.
  • Singh Y. Martin’s physical pharmacy and pharmaceutical sciences. Department of Pharmaceutics Ernest Mario School of Pharmacy Rutgers, the State University of New Jersey, USA, 2013.
  • Archana Kushwaha, Jayanti Jaiswal, Priya Singh. An exhaustive review based on the formulation and evaluation methods behind the development of transdermal drug delivery systems. Research J. Pharm. and Tech. 2017; 10(5): 1531-1538.
  • Alam MA, Al-Jenoobi FI. Commercially bioavailable proprietary technologies and their marketed products. Drug Discovery Today, 2013; 1-14.

Abstract Views: 161

PDF Views: 0




  • Application of Mathematical Models in Drug Release Kinetics of Lagerstroemia Speciosa Extract-phospholipid Complex

Abstract Views: 161  |  PDF Views: 0

Authors

Patel Anar J
Associate Professor, Sal Institute of Pharmacy, Opp. Science City, Ahmedabad 380061, Gujarat,, India
Singh R. P.
NIMS Institute of Pharmacy, Jaipur, Rajasthan,, India
Patel Vaibhav
Anand Pharmacy College, Gujarat,, India
Goswami Shambaditya
NIMS Institute of Pharmacy, Jaipur, Rajasthan,, India

Abstract


The aim of present work is to govern and scrutinize the kinetics of drug release from the complex by employing various mathematical models. A study was done with Lagerstroemia speciosa extract-phospholipid complex, 50 mg/200mg by employing anticipation precipitation technique using soya lecithin and cholesterol as complex forming polymer. In-vitro drug release profile was carried out in phosphate buffer saline, pH 7.4 (900mL) using USP dissolution apparatus II (Paddle) at 50 RPM at an extended time period of 0.5, 0.75, 1, 1.5, 2, 2.5, 3 and 4 hours. The drug release data was obtained, quantitatively correlated and interpreted with various mathematical models viz. Zero order model, first order model, Higuchi model and Korsmeyer-Peppas model and evaluated to understand the kinetics of drug release. The criterion for the most suitable model was based on the high degree of coefficient of correlation of drug release profile was best fitted with Korsmeyer-Peppas model and follows drug release kinetics which is diffusion controlled.

Keywords


Lagerstroemia speciosa extract-phospholipid complex; Diffusion; Coefficient of correlation; Kinetics of drug release.

References