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Enhanced oral bioavailability and anti-diabetic activity of canagliflozin through a spray dried lipid based oral delivery: a novel paradigm.
Singh, Dilpreet; Singh, Amrit Pal; Singh, Drishtant; Kesavan, Anup Kumar; Arora, Saroj; Tiwary, Ashok K; Bedi, Neena.
Affiliation
  • Singh D; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, 143005, India.
  • Singh AP; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, 143005, India.
  • Singh D; Department of Molecular Biology and Biochemistry, Molecular Microbiology Lab, Guru Nanak Dev University, Amritsar, 143005, India.
  • Kesavan AK; Department of Molecular Biology and Biochemistry, Molecular Microbiology Lab, Guru Nanak Dev University, Amritsar, 143005, India.
  • Arora S; Department of Botanical and Environmental Sciences, Guru Nanak Dev University, Amritsar, 143005, India.
  • Tiwary AK; Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala, 147002, India.
  • Bedi N; Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, 143005, India. neena.pharma@gndu.ac.in.
Daru ; 28(1): 191-208, 2020 Jun.
Article in En | MEDLINE | ID: mdl-32034683
AIM: Canagliflozin (CFZ), a novel SGLT II antagonist, exhibits erratic absorption after oral administration. The current study entails development and evaluation of spray dried lipid based formulation (solid SMEDDS) for enhancing oral bioavailability and anti-diabetic activity of CFZ. METHODS: Solid SMEDDS developed through spray drying containing Neusilin US2 as an adsorbent. The formed solid SMEDDS were characterized for physicochemical and solid state attributes. Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM) were used to confirm the spherical morphology. In vitro dissolution, ex vivo permeability and in vivo pharmacokinetic studies were conducted to determine the release rate, permeation rate and absorption profile of CFZ, respectively. Pharmacodynamic studies were done as per standard protocols. RESULTS: The optimized solid SMEDDS exhibited acceptable practical yield and flow properties and is vouched with enhanced amorphization, nanoparticulate distribution and acceptable drug content. The spherical morphology of solid SMEDDS and reconstituted SMEDDS were confirmed in SEM and TEM, respectively. In vitro dissolution studies revealed multi-fold release behavior in CFZ in various dissolution media, whereas, remarkable permeability was observed in jejunum segment of rat intestine. Pharmacokinetic studies of CFZ in solid SMEDDS demonstrated 2.53 and 1.43 fold enhancement in Cmax and 2.73 and 1.98 fold in AUC 0-24h, as compared to pure API and marketed formulation, respectively. Pharmacological evaluation of solid SMEDDS revealed enhanced anti-diabetic activity of CFZ through predominant SGLT II inhibition in rats, as evident from evaluation of biochemical levels, urinary glucose excretion studies and SGLT II expression analysis. CONCLUSION: The current work describes significant improvement biopharmaceutical properties of CFZ in solid SMEDD formulation. Graphical abstract Graphical Abstract: Enhanced oral bioavailability and anti-diabetic activity of canagliflozin through a spray dried lipid based oral delivery: a novel paradigm.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Delivery Systems / Diabetes Mellitus, Experimental / Canagliflozin / Hypoglycemic Agents Type of study: Guideline Language: En Journal: Daru Year: 2020 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Delivery Systems / Diabetes Mellitus, Experimental / Canagliflozin / Hypoglycemic Agents Type of study: Guideline Language: En Journal: Daru Year: 2020 Document type: Article Affiliation country: Country of publication: