Abstract:Efforts directed toward restoring normal metabolic levels by mimicking the physiological insulin secretion, thereby ensuring safety, efficacy, minimal invasiveness and conveniences, are of great significance in the management of type 1 diabetes among children and adolescents. Regardless of the various technologies being discovered in addressing invasiveness and enhancing medication adherence in the management of type 1 diabetes, yet limited success had been observed among children and adolescents. The multiple… Show more
“…As regard method of insulin injection, the present study illustrated that, the majority of the studied children used insulin syringes this may be due to the insulin pump or pen aren't available for all diabetic children or may cause financial load for parents. This finding wasn't in harmony with Zuberi et al (2020) (38) who studied insulin-delivery methods for children and adolescents with type 1 diabetes and his study revealed that, the diabetic alternate delivery method for children and adolescents is insulin pens. Concerning to frequency of insulin injections, the current study revealed that, all the studied children taken insulin injection four times per day.…”
Background: Type 1 diabetes is characterized by deficiency in insulin because of the autoimmune destruction of pancreatic β-cells. Children with type 1 diabetes require lifelong insulin therapy. Non pharmacological methods as Buzzy Bee and Shot Blocker used to reduce children's pain and anxiety. Aim: the present study was aimed to evaluate the effect of shot blockers versus buzzy bee distractor on relieving pain and anxiety during insulin injection among children with type I diabetes.
“…As regard method of insulin injection, the present study illustrated that, the majority of the studied children used insulin syringes this may be due to the insulin pump or pen aren't available for all diabetic children or may cause financial load for parents. This finding wasn't in harmony with Zuberi et al (2020) (38) who studied insulin-delivery methods for children and adolescents with type 1 diabetes and his study revealed that, the diabetic alternate delivery method for children and adolescents is insulin pens. Concerning to frequency of insulin injections, the current study revealed that, all the studied children taken insulin injection four times per day.…”
Background: Type 1 diabetes is characterized by deficiency in insulin because of the autoimmune destruction of pancreatic β-cells. Children with type 1 diabetes require lifelong insulin therapy. Non pharmacological methods as Buzzy Bee and Shot Blocker used to reduce children's pain and anxiety. Aim: the present study was aimed to evaluate the effect of shot blockers versus buzzy bee distractor on relieving pain and anxiety during insulin injection among children with type I diabetes.
“…The typical signs are persistent hunger, frequent urination, and extreme thirst. In those who are genetically susceptible to type II diabetes, obesity is now understood to be the root cause of the condition [30,31] . α‐Glucosidase inhibitors are used in conjunction with other insulin secretagogues to maintain high glycemic control [32,33] .…”
This research work is based on synthesis of eleven novel thiazole derivatives (3 a‐k) of thiophene carbaldehyde. All the synthesized compounds were successfully synthesized, characterized by 1H‐NMR and EI‐MS spectroscopic techniques and finally subjected for their in vitro α‐glucosidase inhibitory activity. Seven derivatives 3 i (IC50=10.21±1.84 μM), 3 b (IC50=11.14±0.99 μM), 3 f (IC50=13.21±2.76 μM), 3 h (IC50=14.21±0.31 μM), 3 k (IC50=15.21±1.02 μM), 3 e (IC50=16.21±1.32 μM), and 3 c (IC50=18.21±1.89 μM), in the series displayed excellent inhibitory potential better than the standard acarbose. However, two compounds 3 g (IC50=33.21±1.99 μM) and 3 d (IC50=42.31±2.12 μM) showed significant activity while two compounds 3 j and 3 a were found less active with IC50 values of 82.31±0.31 and 88.36±1.21 μM respectively. Additional research revealed that the compounds are not exhibiting any cytotoxic effects. The molecular docking study of these derivatives showed their good binding potential for α‐glucosidase active site with excellent interactions and docking scores.
“…The enzyme is also located in the lining of small intestine where it plays a crucial role in the final stage of glucose metabolism. The enzyme functions by catalyzing the α-glucosidic disaccharide and oligosaccharide bonds owing to the presence of duplicated glycoside hydrolase domains (GH31). , Besides carbohydrate digestion, α-glucosidase enzyme is also essential for numerous biological processes such as degradation of lysosomal glycoconjugates and the modification of post-translational glycoproteins . The enzymatic activity of α-glucosidase is significant in the management of type 2 diabetes mellitus (T2DM) as its inhibition retards the rate of breakdown of starch.…”
Section: Introductionmentioning
confidence: 99%
“… 24 , 25 Besides carbohydrate digestion, α-glucosidase enzyme is also essential for numerous biological processes such as degradation of lysosomal glycoconjugates and the modification of post-translational glycoproteins. 26 The enzymatic activity of α-glucosidase is significant in the management of type 2 diabetes mellitus (T2DM) as its inhibition retards the rate of breakdown of starch. It helps in regulating the postprandial hyperglycemia.…”
In the present work, 2-imino-1,3-thiazolines featuring
highly fluorinated
fragments were synthesized through a straightforward cyclization of
diversely substituted thioureas with 2-bromo-1-(4-fluorophenyl)ethan-1-one.
The target compounds were obtained in good yields, and structures
were established by FTIR and 1H- and 13C NMR
spectroscopic methods. The in vitro biological assay revealed that
all the compounds significantly obstruct the α-glucosidase.
Compound 6d (3-fluoro-N-(3-(2-fluorophenyl)-4-(4-fluorophenyl)thiazol-2(3H)-ylidene)benzamide) showed the highest antidiabetic potential
with an IC50 value of 1.47 ± 0.05 μM. In addition,
computational analysis revealed the binding energy of −11.1
kcal/mol for 6d which was lower than the positive standard,
acarbose (−7.9 kcal/mol). Several intermolecular interactions
between the active site residues and 6d highlight the
significance of 2-imino-1,3-thiazoline core in attaining the potent
efficacy and making these compounds a valuable pharmacophore in drug
discovery.
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