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13 protocols using pvpva64

1

Polymer Sorption Behavior Characterization

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Four different molecular weights (grades) of the polymer HPC (HPC-UL with 20,000 g/mol, HPC-SSL with 40,000 g/mol, HPC-SL with 100,000 g/mol, and HPC-L with 140,000 g/mol) were provided by Nisso Chemical Europe GmbH (Düsseldorf, Germany). The APIs fenofibrate (98% purity) and itraconazole (99% purity) were obtained from VWR International GmbH (Darmstadt). The solvents for DVS analysis (ethanol, acetone, and cyclohexane) were obtained in chromatographic grade from VWR International GmbH (Darmstadt), PVPVA64 was provided by BASF SE (Ludwigshafen, Germany). Water required for sorption experiments was filtered and deionized prior use.
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2

Formulation Development of Pharmaceutical Dosage Forms

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ITR, MgSt, and SSF were provided by Johnson & Johnson Pharmaceutical Research and Development (Beerse, Belgium). Aerosil ® 200 was purchased from Evonik Industries (Essen, Germany). Microcrystalline cellulose (MCC, Vivapur ® 200) was given by JRS Pharma (Rosenberg, Germany). Mannitol (Pearlitol ® 400DC) was a kind gift from Roquette Pharma (Lestrem, France). PVPVA64 and Kollidon ® CL were supplied by BASF (Ludwigshafen, Germany).
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3

Formulation of CEL film III

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CEL form III was provided as a gift sample by Jubilant Generics Ltd. (Noida, Uttar Pradesh, India). PVP-VA 64, manufactured by BASF (Germany) and HPMCAS-MF grade, manufactured by Shin Estu (Japan) was generously provided by Signet Chemical Corporation Pvt. Ltd. (Mumbai, India). NaOH and KOH were procured from Himedia Laboratories Pvt. Ltd. (Mumbai, India). All other chemicals used in the experiments were of analytical grade and used as such.
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4

Formulation Development for Fenofibrate and Simvastatin

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The APIs fenofibrate (98% purity) and simvastatin (98% purity), ethanol (96% purity) for spray drying and the buffer salts for the dissolution media were purchased from VWR International GmbH (Darmstadt). The two HPC polymers HPC-UL (20.000 g/mol) and HPC-SSL (40.000 g/mol) were provided by Nisso Chemical Europe GmbH (Düsseldorf, Germany). The polymer HPMCAS-M was obtained from ShinEtsu (SE Tylose GmbH & Co. KG, Wiesbaden, Germany), PVPVA64 was obtained from BASF SE (Ludwigshafen, Germany). Water required for dissolution experiments was filtered and deionized prior use.
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5

Optimized Glycyrrhetinic Acid Formulation

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OA was purchased from Wuhan Dahua Pharmaceutical Co., Ltd. (Wuhan, Hubei). Soluplus® and PVP VA64 were purchased from BASF Co., Ltd. (Shanghai, China). PEG 6000 was obtained from Beijing Fengli Jingqiu Pharmaceutical Co., Ltd. (Beijing, China). Sodium dodecyl sulfate (SDS) was purchased from Tianjin Bodi Chemical Holding Co., Ltd. (Tianjin, China). H3PO4 was obtained from Tianjin Kemiou Chemical Reagent Co., Ltd. (Tianjin, China). Glycyrrhetinic acid was obtained from China's food and drug administration. Methanol, Methyl tert-Butyl Ether of HPLC grade was purchased from Thermo Fisher Scientific (Shanghai, China). Ammonium acetate (HPLC grade) was purchased from Dikma Technology Inc. (Beijing, China).
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6

Multifaceted Nanoformulation for Cancer Treatment

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FLQY2 was synthesized by our laboratory (purity  > 98%) [32 ]. Soluplus®, Poloxamer 407, PVP Va64, and HS 15 were purchased from BASF Co., Ltd (Shanghai, China). PEG4000, PEG6000, and Irinotecan hydrochloride were obtained from Aladdin Bio-chem Technology Co., Ltd (Shanghai, China). Paclitaxel Injection (Albumin-Bound) was purchased from Kelun Pharmaceutical Co., Ltd (Yueyang, China). Human colon cancer cells (HCT 116) and human pancreatic cancer cells (MIA PaCa-2) were acquired from the National Collection of Authenticated Cell Cultures (Shanghai, China). McCoy’s 5A medium and DMEM medium were obtained from SIGMA (Shanghai, China). FBS was purchased from Gibco (Shanghai, China). Penicillin–streptomycin solution (100 ×) was obtained from Solarbio Co., Ltd (Beijing, China). Acetonitrile and ultrapure water for HPLC-grade were purchased from Merck (Darmstadt, Germany). HPLC-grade formic acid and ammonium acetate were purchased from CNW (Shanghai, China). All the other chemicals were of analytical grade and commercially available.
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7

Olanzapine Solid Dispersion Formulation

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Olanzapine [molecular weight (Mw) = 312.43 g/mol, density (ρ) = 1.30 g/cm3] was purchased from Myjoy Ltd. (India); PVP K30 (Mw = 41.550 g/mol, ρ = 1.16 g/cm3), PVPVA 6:4 (Mw = 57.500 g/mol, ρ = 1.17 g/cm3), and SLP (Mw = 118.000 g/mol, ρ = 1.20 g/cm3) were kindly donated by BASF Chemicals (Germany). Methanol (analytical grade) was obtained from Sigma–Aldrich (UK) . Phosphate buffer, pH 6.8 (Ph Eur), used in the dissolution studies was prepared with potassium dihydrogen orthophosphate (Fischer Scientific, UK) and sodium phosphate dibasic (Sigma–Aldrich).
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8

Trans-Resveratrol Formulation Development

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Trans-resveratrol was provided by Ningbo Liwah Pharmaceutical Co., Ltd. (Ningbo, China). Eudragit E PO (powder form of a cationic copolymer based on dimethylaminoethyl methacrylate, butyl methacrylate, and methyl methacrylate with a ratio of 2:1:1), polyvinylpyrrolidone K30 (PVP K30), and polyvinylpyrrolidone vinyl acetate 64 (PVP VA 64) were kindly donated by BASF (Ludwigshafen, Germany). Hydroxylpropylmethyl cellulose (HPMC 6 cp) and hydroxylpropyl cellulose (HPC-L) were kindly donated by Shin-Etsu Chemical Co., Ltd. (Tokyo, Japan), and Nippon Soda Co., Ltd. (Tokyo, Japan), respectively. Eudragit E/HCl (neutralized Eudragit E with hydrochloric acid) powder was prepared as previously reported [29 (link)]. All organic solvents of high-performance liquid chromatography (HPLC) grade were purchased from J.T. Baker (Phillipsburg, NJ, USA). All reagents used were of analytical grade and purchased from Sigma-Aldrich Co., Ltd. (St Louis, MO, USA) or Daejung Chemicals and Metals Co., Ltd. (Siheung-si, Korea).
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9

Dissolution Study of Pharmaceutical Compounds

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Itraconazole, naproxen and phenytoin were obtained from Chemie Brunschwig (Basel, Switzerland). Cinnarizine, ketoconazole, probenecid, sodium chloride, sodium hydroxide and sodium phosphate dihydrate were obtained from Sigma-Aldrich (Steinheim, Germany). Dimethyl sulfoxide was obtained from VWR Chemicals (Søborg, Denmark). SIF powder was obtained from Biorelevant (South Croydon, UK). HPMCAS-L was gifted by Dow Wolf Cellulosics (Bomlitz, Germany) and PVPVA64 was obtained from BASF (Basel, Switzerland). All materials were used as received.
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10

Preparation and Characterization of Poorly Soluble Drug Formulations

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PXCM and PHY were purchased from TCI Chemicals (Tokyo, Japan) and Spectrum Chemical (New Brunswick, NJ, USA), respectively. RTV was provided by Abbott Laboratories (now AbbVie Inc., North Chicago, IL, USA). PVP-VA64 (Tg = 108 °C) was purchased from BASF (Ludwigshafen, Germany). All model compounds are poorly soluble drugs as per the biopharmaceutics classification system (BCS) [50 (link)], as detailed in Table 2. HPLC-grade methanol (MeOH) and acetonitrile (ACN) were purchased from Honeywell (Charlotte, NC, USA). Tri-fluoro acetic acid (TFA) and KH2PO4 were purchased from Fisher (Hampton, NH, USA). All materials were used as received. All water (H2O) used was MilliQ grade with 18.2 MΩ resistance.
Physical mixtures were prepared by weighing an appropriate amount of each component into a scintillation vial and mixed with acoustic mixing at 50 G for 2 min using a LabRAM II (Resodyn Corporation, Butte, MT, USA).
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