Formulation development of sublingual films and tablets of tacrolimus for bioavailability enhancement

dc.contributor.guideGopinath, S
dc.coverage.spatialTacrolimus
dc.creator.researcherJisha Mohanan
dc.date.accessioned2024-11-19T04:36:24Z
dc.date.available2024-11-19T04:36:24Z
dc.date.awarded2024
dc.date.completed2024
dc.date.registered2016
dc.description.abstractnewlineTacrolimus is the most successfully used immunosuppressant today for the prevention of allograft rejection The drug is classified under BCS class II with low solubility and high permeability and has shown poor pharmacokinetic properties as well as bioavailability So the aim of the study was to develop sublingual fast dissolving dosage forms ie films and tablets of tacrolimus to improve its bioavailability In the first phase of the work in order to increase the solubility of tacrolimus inclusion complexes with beta cyclodextrin were prepared by utilizing kneading method and were subjected to various in vitro evaluations The inclusion complexes showed more than fourfold increase in aqueous solubility In the second phase the optimized inclusion complexes were further developed into fast dissolving tablets by direct compression method In the third phase films were developed with inclusion complexes using solvent casting technique with HPMC E5 as film forming polymer The design and optimization of films were achieved by Design of Experiment approach using central composite design The developed tablets and films were characterized by different in vitro evaluations and they showed satisfactory performances on all evaluations The results of stability analysis revealed that the prepared formulations retained their stability under accelerated storage conditions as per ICH guidelines The optimized formulations were subjected to in vivo bioavailability studies using New Zealand white rabbits and showed enhancement in bioavailability in comparison with oral marketed formulation Thus the present study has demonstrated the successful utility of sublingual route for the administration of the life saving drug tacrolimus
dc.description.noteChapter 1 Introduction p.1-38 Chapter 2 Review of Literature p.39-61 Chapter 3 Aim and Objectives p.62 Chapter 4 Methodology p.63-100 Chapter 5 Results 101-156 Chapter 6 Discussion p.157-171 Chapter 7 Summary, Conclusion and Recommendations for Future Studies p.172-176.
dc.format.accompanyingmaterialNone
dc.format.dimensions15 cms
dc.format.extent1-176
dc.identifier.urihttp://hdl.handle.net/10603/601641
dc.languageEnglish
dc.publisher.institutionCollege of Pharmacy
dc.publisher.placeChennai
dc.publisher.universitySri Ramachandra Institute of Higher Education and Research
dc.relation
dc.rightsself
dc.source.universityUniversity
dc.subject.keywordClinical Pre Clinical and Health
dc.subject.keywordPharmacology and Pharmacy
dc.subject.keywordPharmacology and Toxicology
dc.titleFormulation development of sublingual films and tablets of tacrolimus for bioavailability enhancement
dc.title.alternative
dc.type.degreePh.D.

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