Gliclazide in Binary and Ternary Systems Improves Physicochemical Properties, Bioactivity, and Antioxidant Activity.
Muhammad IbrahimShehla MunirSarfraz AhmedAdeel Hussain ChughtaiWaqas AhmadJallat KhanMogana Das MurteyHira IjazSuvash Chandra OjhaPublished in: Oxidative medicine and cellular longevity (2022)
The poor solubility of the antidiabetic drug gliclazide (Glc) is due to its hydrophobic nature. This research is aimed at improving Glc's solubility and drug release profile, as well as at investigating additional benefits such as bioactivity and antioxidant activity, by forming binary complexes with HP β CD at different w / w ratios (1 : 1, 1 : 2.5, 1 : 4, and 1 : 9) and ternary complexes with HP β CD and Tryp at 1 : 1 : 1, 1 : 1 : 0.27, 1 : 2.5 : 0.27, 1 : 3.6 : 3.6, 1 : 4 : 1, and 1 : 9 : 1, respectively. Complexes were prepared by the physical mixing (PM) and solvent evaporation (SE) methods. The prepared inclusion complexes were meticulously characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), and attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectra. To verify our findings, the inclusion complexes were evaluated by equilibrium solubility, in vitro drug release profile, kinetic models, and antidiabetic and antioxidant activities in animal models. Our results demonstrated that the solubility and drug release profile were found to be enhanced through binary as well as ternary complexes. Notably, ternary complexes with a ratio of 1 : 9 : 1 showed the highest solubility and drug release profile compared to all other preparations. Data on antioxidant activity indicated that the ternary complex had the higher total antioxidant status (TAS), superoxide dismutase (SOD), and catalase (CAT) activity than the binary complex and Glc alone, in contrast to the diabetic group. In vivo antidiabetic activity data revealed a high percentage reduction in the blood glucose level by ternary complexes (49-52%) compared to the binary complexes (45-46%; p ≤ 0.05). HP β CD and Tryp provide a new platform for overcoming the challenges associated with poorly soluble Glc by providing greater complexing and solubilizing capabilities and imparting ancillary benefits to improve the drug's antidiabetic and antioxidant activities.
Keyphrases
- drug release
- drug delivery
- ionic liquid
- blood glucose
- electron microscopy
- reduced graphene oxide
- type diabetes
- high resolution
- electronic health record
- computed tomography
- magnetic resonance
- blood pressure
- machine learning
- high throughput
- physical activity
- mass spectrometry
- mental health
- dna damage
- nitric oxide
- risk assessment
- gold nanoparticles
- molecular dynamics simulations
- metabolic syndrome
- molecular dynamics
- nk cells
- single cell
- insulin resistance
- particulate matter
- weight loss
- data analysis
- contrast enhanced
- dna repair