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33 protocols using lactose monohydrate

1

Flufenamic Acid Polymorphs Characterization

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In this study, Flufenamic acid (FA) polymorphic forms were used, as previously studied and considered to be bench stable. Flufenamic acid {Sigma-Aldrich, UK} forms I (FA I) and III (FA III) were prepared as previously described. [13] (link) Excipients included Ac-Di-SoL® (croscarmellose sodium {FMC Biopolymer, UK}) and lactose monohydrate {Sigma-Aldrich, UK}. Forms I and III were independently dispensed as a 17% premix in lactose monohydrate to assist with the weighing of very small quantities. These compounds were selected for their wide use within the pharmaceutical industries.
Additional consideration was given to their characteristic Raman features, for example lactose is a good Raman scatterer whereas Ac-Di-SoL® lacks Raman features and is very fluorescent.
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2

β-Galactosidase Assay Using Lactozym

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A commercial preparation of β-galactosidase from Kluyveromyces lactis, Lactozym 3000 L HP-G (Novo Nordisk A/S, Bagvaerd, Denmark), was used. The chemicals used to prepare the reaction media and standard solutions were lactose monohydrate and glucose anhydrous from Merck (Darmstadt, Germany); galactose, melezitose and bovine serum albumin (BSA), fraction V, from Sigma (St. Louis, MI, USA) and raffinose from Panreac (Chicago, IL, USA). Cellulose acetate with 38.9% acetyl content was purchased from Sigma. The other chemicals used were all of analytical grade. Deionized water was used for preparation of media and membrane-rinsing solutions, while for chromatographic standards, Milli-Q ultrapure water (through Q-POD unit) was used.
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3

Melatonin Polymer Characterization

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Melatonin (Mw: 232,28, λmax: 278 nm) was purchased from Tokyo Chemical Industry (Tokyo, Japan). The new polymers (neat PLA, PLA/PEAd [90/10], PLA/PEAd [75/25], PLA/PBAd [90/10], and PLA/PBAd [75/25]) were kindly donated from the Laboratory of Professor Dimitrios Bikiaris, which is part of the Laboratory of Chemistry and Technology of Polymers and Dyes, in the Department of Chemistry of Aristotle University of Thessaloniki, Greece. HPMC K15M was supplied from Sigma-Aldrich (Steinheim, Germany). Alginic acid sodium salt (low viscosity) and Avicel PH 102 were obtained from Alfa Aesar GmbH & Co. KG (Karlsruhe, Germany). Lactose monohydrate was purchased from Merck (Darmstadt, Germany), whereas magnesium stearate was obtained from Riedel-De Haen (Hannover, Germany). All chemicals were of reagent grade and were used in the study without further purification.
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4

Phenotypic Characterization of Lactic Acid Bacteria

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The selected strains (OD600 = 1) were inoculated into mMRS broth (1%) to evaluate growth at different temperatures (15, 28, 37 and 45 °C), pH (3.5, 4.5 and 6.5) and salt (4, 6 and 8%) conditions. Each condition was tested separately. The abilities of the strains to ferment various carbohydrates were performed with different sugars including D (+) glucose monohydrate (Sigma-Aldrich), D (-) fructose (Merck), D (+) galactose (Fluka), lactose monohydrate (Merck), sucrose (Merck), maltose monohydrate (Merck), L (+) rhamnose monohydrate, raffinose (Difco), D (-) mannitol (Merck), D (+) mannose (Fluka), D (-) arabinose (Fluka) and D (+) xylose (Sigma Aldrich). For that purpose, each filter-sterilized sugar solution (1%, w/v) was added separately to the tubes including MRS broth prepared without meat extract and glucose. Then each strain (OD600 = 1) was inoculated individually into each tube. Chlorophenol red (0.004%, w/v) was used as the indicator. The control broth was prepared without any sugar.
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5

Tris-Egg Yolk Extender Preparation

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Tris-egg yolk extender was prepared freshly by mixing 1.363 g Tris-aminomethane (Merck, CAS Number: 108382, Darmstadt, Germany), 0.762 g citric acid (CAS Number: 77-92-9 100241-Merck Millipore), 1.5 g lactose monohydrate (Merck CAS Number: 1.07660), and 2.7 g D-(+)-raffinose pentahydrate (Merck, CAS Number: 512-69-6), 0.5 g D(-)-fructose (Merck, CAS Number: 57-48-7 104007) was dissolved in 80 mL double-distilled water and homogenized with a magnetic stirrer for 10-15 min [8 (link)]. The extender osmolarity was 295 mOsm/L (WESCOR model 5500, INC, USA). The solution was heated to 100°C for a few minutes and cooled to room temperature (26°C), after which it was mixed with 0.1 g penicillin G (Meiji Seika Co., Tokyo, Japan) and 0.1 streptomycin sulfate (Meiji). The mixture was homogenized again for 10-15 min. Egg yolk (20 mL) was dissolved in 80 mL of the mixture, centrifuged 492 × g for 15 min, the supernatant was used as an extender while the precipitate was removed [2 (link)].
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6

Budesonide Sustained-Release Formulations

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Budesonide (BU) was acquired from Jaber Ebne Hayyan Pharmaceutical Company (Tehran, Iran). Lactose monohydrate and Avicel pH 102 were obtained from Merck, Frankfurt, Germany. Polyvinylpyrrolidone (PVP K30) (Rahavard Tamin, Saveh, Iran), eudragit S PO, (Evonik Industries AG, Hanau, Germany), eudragit L PO, (Evonik Industries AG, Hanau, Germany), eudragit RS PO, (Evonik Industries AG, Hanau, Germany), talc, (Merck, Frankfurt, Germany), triethyl citrate (TEC) (Merck, Frankfurt, Germany), chitosan (medium-molecular-weight, 75–85% deacetylated) (Sigma-Aldrich, St. Louis, USA), three polyphosphate (Merk, Frankfurt, Germany), acetic acid (Dr. Mojallaly, Tehran, Iran), ethanol (Dr. Mojallaly, Tehran, Iran), isopropyl alcohol (2-propanol) (Dr. Mojallaly, Tehran, Iran) and sodium lauryl sulfate (SLS) (Scharlau, Barcelona, Spain) were utilized. All other reagents and solvents were of analytical grades.
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7

Formulation and Evaluation of Glibenclamide Solid Dosage Forms

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Glibenclamide was obtained from Mahban Chemi Co. (Tehran, Iran). Coarse granular microcrystalline cellulose (Avicel) (Mingtai Chemical, Bah-Dern City, Taiwan), sodium starch glycolate (Yung Zip Chemical, Taichung City, Taiwan), nm-sized amorphous silicon dioxide (Mingtai Chemical, Bah-Der City, Taiwan), Polyoxyethylene (40) Stearate (MYRJ 52) (Croda, Trappes, France), polyvinylpyrrolidone (PVP) and Cremophor® RH 40 (BASF, Germany), polyethylene glycol (PEG 200 and 400), glycerine, propylene glycol (PG), polyoxyethylenlaurylether (Brij35), lactose monohydrate (Pharmaceutical grade), sodium hydroxide and potassium dihydrogen phosphate were obtained from Merck, (Darmstadt, Germany). Diethylene glycol monoethyl ether (transcutol P) was supplied by Gattefosse (Lyon, France).
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8

Tablet Dissolution Experiments with Griseofulvin

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The following chemicals were used for the tablet dissolution experiments. Pemulen TR2 NF was kindly provided by Lubrizol Advanced Materials (Brussels, Belgium). According to the supplier, the polymer consists of poly (acrylic acid) cross-linked with allylpentaerytritol and contains 52–62 wt% of carboxylic acid groups. Pemulen is hydrophobically modified with grafted C10-C30 alkyl-chains. Griseofulvin was purchased from Sigma (Steinheim, Germany) and used as provided.
Sodium dodecyl sulphate (SDS) was purchased from VWR International (Poole, England). The CMC for SDS is 8.3 mM in pure water [23 ] and was determined, with a tensiometer and a de Noüy ring, to 1.8 mM at 37°C in 0.1 M phosphate buffered solution, pH 7.2. For tableting, lactose monohydrate from Merck (Darmstadt, Germany) was used as supplied and talc and magnesium stearate were of analytical grade.
The following chemicals were used to prepare the simulated intestinal fluid. Sodium taurocholate (NaTC) was purchased from TCI (Zwijndrecht, Belgium). Lecithin from soybeans and sodium oleate was acquired from VWR International (Leuven, Belgium and Fonteray sous Bois, France). Glycerol monooleate was purchased from Grindsted Products (Copenhagen, Denmark) and maleic acid was acquired from Sigma (Steinheim, Germany). NaOH and NaCl were of analytical grade. All chemicals were used as received.
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9

Furosemide Formulation Development and Evaluation

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Furosemide was purchased from Sigma-Aldrich (Steinheim, Germany). The different grades of Eudragit ® polymers L 100-55, L100, S100, RL100, RS were purchased from Rohm GmbH Pharma Polymers (Darmstadt, Germany). Poly(ethylene oxide) (M r 0.9 × 10 6 , 4 × 10 6 , 5 × 10 6 , 7 × 10 6 ), polyvinylpyrrolidone (PVP, average MW 10.000), and Sodium Lauryl Sulfate (SLS) were purchased from Sigma-Aldrich (Steinheim, Germany), lactose monohydrate was purchased from Merck, whereas magnesium stearate was obtained from Riedel-De Haen (Hannover, Germany). Lasix ® 40 mg tablets are commercially available and were purchased from a local drug store. All chemicals were of reagent grade and were used in the study without further purification.
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10

HPLC Analysis of Milk Oligosaccharides

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HPLC grade acetonitrile and isopropanol were purchased from Thermo Fisher Scientific. Triethylamine (≥99%) was obtained from Sigma‐Aldrich. 2’‐FL (>95%) was purchased from Carbosynth (Berkshire, UK). The standard for 3‐FL (99.7%) was kindly provided by Danisco Sweeteners Oy (Kantvik, Finland). Lactose monohydrate and sucrose were both purchased from Merck (Darmstadt, Germany). Water was purified in a Milli‐Q water purification system from Millipore (Molsheim, France).
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