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Acarbose

Manufactured by Merck Group
Sourced in United States, Germany, India, China, Italy, France, Australia, Singapore, United Kingdom, Spain, Brazil

Acarbose is a prescription medication used to help manage blood sugar levels in individuals with diabetes. It works by slowing the breakdown and absorption of carbohydrates in the digestive system, which can help control postprandial (after-meal) blood glucose levels. Acarbose is an enzyme inhibitor that targets alpha-glucosidase, an enzyme responsible for breaking down complex carbohydrates.

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376 protocols using acarbose

1

Evaluation of Antioxidant and α-Glucosidase Inhibitory Activities

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Standards of the determined substances: acarbose, chlorogenic acid, epicatechin, quercetin, kaempferol, and rutin, were obtained from Sigma-Aldrich (St. Louis, MO, USA).
The reagents used in the conducted studies are as follows: α-D-glucopyranoside (pNPG), α-glucosidase, acarbose, 2,2-Diphenyl-1-picrylhydrazyl, TPTZ (2,4,6-tripyridyl-S-triazine) and Iron (III) chloride hexahydrate (FeCl3x6H2O), Folin–Ciocalteu’s phenol reagent, sodium carbonate, 2,4,6-tris(2-pyridyl)-1,3,5-triazine (TPTZ, C18H12N6), iron(III) chloride hexahydrate (FeCl3·6H2O), Trolox, α-cyclodextrin (α-CD), β-cyclodextrin (β-CD), and γ-cyclodextrin (γ-CD) were supplied by Sigma-Aldrich, St. Louis, MO, USA. Methanol, isopropanol, and acetone (Super Purity Solvent, Methanol 215 SPS) were supplied by ROMIL Ltd., Cambridge, England.
High-quality pure and ultra-high-quality pure water were prepared using a Direct-Q 3 UV Merck Millipore (Burlington, MA, USA) purification system.
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2

Phytochemical and Enzyme Inhibition

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Different chemicals reagents used in this study were purchased from different chemical suppliers. Quercetin, 2, 2-Diphenyl-1-picrylhydrazyl (DPPH) and 2, 2′-Azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS), α-amylase from procine pancreas (Type VI-B), Tyrosinase from mushroom, Lipase from procine pancreas (Type II), 4-nitrophenyl butyrate (p-NPB), Orlistat, Acarbose, α-glucosidase from Saccharomyces cerevisiae (Type-I), p-Nitrophenyl-α-D-glucopyranoside (p-NPG), Sodium carbonate, Kojic acid, l-3,4-dihydroxyphenylalanine (L-DOPA), N-Succinyl-Ala-Ala-p-nitroanilide (AAAPVN), Porcine pancreatic elastase (PPE), Galantamine, Acetylcholinesterase (AChE), Butyrylcholinesterase (BChE), Acetylcholine iodide, Butyrylcholine iodide, 5,5′-dithiobis-(2-nitrobenzoic acid) (DTNB), Acetonitrile (LC-MS grade), Methanol (LC-MS grade), Formic acid (analytical grade), and Acarbose from Sigma-aldrich (USA). The 3,5-Dinitrosalicylic acid (DNSA) from HIMEDIA (India) and Sodium-potassium tartrate from Merc (Germany). Methanol, Sodium Hydroxide, Dimethyl sulfoxide (DMSO), and Starch from Fisher Scientific (India). Aluminum Chloride, Hexane and Gallic Acid from LOBA Chemie (India).
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3

Vindoline Assay with Rat Insulin and TNF-α Detection

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Vindoline was purchased from Best of Chemicals Sciences (Shirley, NY, USA; purity > 98%). The rat insulin and TNF-α Elisa kits were obtained from Biocom BioAfrica (Centurion, South Africa) while the diaminofluorescin-FM diacetate and dihhyroethidium fluorescence probes were purchased from the Thermofisher Scientific group (Waltham, MA, USA). The cell proliferation reagent WST-1, acarbose and all the solvents/chemicals used for plant extraction and antioxidant analysis were obtained from the Merck-group (Sigma Aldrich, Johannesburg, South Africa).
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4

Antioxidant and Antidiabetic Potential of Lotus Leaves

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Lotus leaves (Nelumbo nucifera Gaertn) were collected from Meishan, Sichuan Province, China. Lotus leaves were dried by hot wind at 75 °C for 7 h according to a previous study [6 (link)], and then pulverized into powder.
Choline chloride, ethylene glycol, 2-diphenyl-1-picrylhydrazyl (DPPH), 3-ethylbenzthiazoline-6-sulphonic acid (ABTS), hydroxytoluene (BHT), 4-nitrophenyl β-D-glucopyranoside (pNPG), α-glucosidase (10 U/mg), α-amylase (1000 U/mg), acarbose, 1-phenyl-3-methyl-5-pyrazolone (PMP), vitamin C, and soluble starch were purchased from Merck (Merck Ltd., Darmstadt, Germany).
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5

Phytochemical Analysis and Bioactivity Evaluation

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All chemicals, including Folin-Ciocalteu’s phenol reagent, tannic acid (Ph Eur purity), aluminium chloride hexahydrate (AlCl3 × 6 H2O; Ph Eur purity), 1,1-diphenyl-2-picrylhydrazyl radical (DPPH; 95% purity), 2,2′-azino-bis (3-thylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS; 98% purity), 2,2′-azobis (2-methylpropionamidine) dihydrochloride (AAPH; 97% purity), ferrozine (97% purity), hydroxylamine hydrochloride (98% purity), iron (III) chloride (FeCl3 × 6H2O; 97% purity), iron (II) sulfate heptahydrate (FeSO4 × 7H2O; 99% purity), trolox (97% purity), quercetin (98% purity), rutin (99% purity), tannic acid (98% purity), bovine serum albumin, glucose, fructose, sodium azide, 4-nitrophenyl β-D-glucopyranoside (PNPG), acarbose, and the analytical-grade solvents ethyl acetate (AcOEt; 99.8% purity), iron (II) chloride (FeCl2 × 4H2O; 99% purity), polyvinylpyrrolidone (PVP), potato starch, sodium carbonate, the enzymes α-amylase from a hog pancreas (50 U/mg), and α-glucosidase from Saccharomyces cerevisiae (≥10 U/mg protein), as well as the analytical grade solvents were purchased from Merck (Darmstadt, Germany).
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6

Chromatographic Separation and Analysis of Glucosides

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LiChroprep Rp-18 (40–63 μm, Merck, Darmstadt, Germany), silica gel (200–300 mesh, Qingdao Haiyang Chemical Co. Ltd., Qingdao, China) and Sephadex LH-20 (25–100 μm, GE Healthcare Bio-Science AB, Uppsala, Sweden) were used as a stationary phase for column chromatography (CC). Precoated silica gel GF254 plates, 0.2–0.25 mm thick (Qingdao Haiyang Chemical Co., Qingdao, China), were used for thin layer chromatography (TLC) analysis, spots were visualized under a UV radiation by spraying with a sulfuric acid: ethanol (1:9, v/v) solution followed by heating. 4-Nitrophenyl-α-D-glucopyranoside (pNPG), α-glucosidase, quercetin and acarbose were purchased from sigma chemical (Merck KGaA, Darmstadt, Germany).
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7

Evaluation of Antioxidant and Enzyme Inhibition Potential

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Acarbose, acetic acid, 2,2′-azobis(2-amidinopropane) dihydrochloride (AAPH), bovine serum albumin (BSA), dichlorofluorescin diacetate (DCFH-DA), dimethylsulfoxide, fluorescein, α-glucosidase (EC 3.2.1.20, Saccharomyces cerevisiae type I, ≥10 Units/mg protein), 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (trolox), luteolin, methanol, p-nitrophenyl-α-D-glucopyranoside (p-NPG), thiazolyl tetrazolium bromide, and vernodalol were purchased from Merck Life Science S.r.l. Milan, Italy. The purity of the standards was ≥97%, while for the other compounds it was at least of analytical grade. Specifically, the purity of luteolin was 98% and that of vernodalol was 95%.
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8

α-Glucosidase Inhibition Assay Protocol

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Ethanol 96%, citric acid, acetic acid, trichloroacetic acid (TCA), formic acid, acetonitrile (ACN), sodium phosphate salts (Na2HPO4, NaH2PO4), p-nitrophenyl-α-D-glucopyranoside (p-NPG), α-glucosidase from rice, sodium carbonate, acarbose and cyaniding were purchased from Merck (Darmstadt, Germany). All reagents used in the experimental part were of analytical purity.
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9

Enzymatic Characterization of α-Glucosidase

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α-Glucosidase (EC 3.2.1.20) from Saccharomyces cerevisiae (750 UN) and p-nitrophenyl-α-d-glucopyranoside were obtained from Sigma Chemical Co. (St. Louis, MO, USA). Acarbose and dimethylsulfoxide were purchased from Merck (Darmstadt, Germany). Silica gel 60, 40–63 µm (230–400 mesh ASTM), for column chromatography was purchased from Scharlau (Barcelona, Spain). Analytical and preparative TLC were carried out on precoated Kiesegel 60F254 or RP-18F254 plates (0.25 or 0.5 mm thickness) (Merck, Germany). Other chemicals were of the highest grade available.
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10

Starch Hydrolysis and Inhibition Assay

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The research materials used were purchased from Merck: soluble starch (from potato, ACS grade), 3,5-dinitrosalicylic acid (DNS) reagent (≥98%, HPLC grade), acarbose (≥95%), glacial acetic acid (pharmaceutical primary standard), alpha amylase from Aspergillus oryzae (≥150 units/mg protein), chitosan (low molecular weight, 50,000–190,000 Da), sodium tripolyphosphate (NaTPP, technical grade, 85%), D-(+) glucose (analytical standard), quercetin (≥95% HPLC, solid), ascorbic acid (pharmaceutical secondary standard), sodium hydroxide (≥98%, pellets, anhydrous), potassium sodium tartrate tetrahydrate (≥99%), sodium sulfite (≥98%), and sodium acetate (anhydrous, ≥99%). The R. tuberosa L. root powder was obtained from UPT Materia Medica Batu, East Java, Indonesia, enclosed with determination letter of species.
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