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13 protocols using poloxamer 407 pluronic f127

1

Poloxamer-Based Hydrogel Formulations

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Poloxamer 407 (Pluronic F127) and Pluronic L 31 were purchased from Sigma-Aldrich-Chemie (Steinheim, Germany). Poloxamer-based binary hydrogels were prepared by the cold method [38 (link)]. To prepare blank poloxamer-based hydrogel (B-PbH), accurately weighed amounts of P127 (20% w/w) and P31 (1% w/w) were added to purified water cooled to 4 °C. The mixture was kept in the refrigerator at least 24 h and periodically stirred until a clear, homogenous solution was obtained, thus ensuring the complete dissolution of the poloxamers. Poloxamer-based binary formulation containing OEO (5% w/w) was prepared by the same method, adding the volatile oil to the cold aqueous solution of the two poloxamers under continuous stirring until a clear, homogenous hydrogel was obtained.
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2

Lipid-based Nanocarrier Formulation

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Hydrogenated palm oil, (Softisan 154 or S154) a gift from Condea (Witten, Germany), and stearic acid (SA, Sigma Aldrich, USA) were the lipids used in this study. Water soluble surfactants used were polioxiethylene-20-sorbitan monooleate (Tween 80- Sigma Aldrich, USA), Poloxamer407 (Pluronic F127, Sigma Aldrich, USA). Furthermore, lipo-soluble surfactants used were Sorbitanmonooleate (Span 80, Sigma Aldrich, USA), and soy lecithin (Sigma-Aldrich). Doxycycline hyclate (Sigma-Aldrich). Water used in our study was distilled twice and purified by an appropriate filter.
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3

Thermosensitive Hydrogel Formulations

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Briefly, to prepare thermo-sensitive hydrogel samples, required amount of poloxamers and additives were separately dissolved in 10 g of saline as a solvent (Taiwan Biotech, Taoyuan, Taiwan) and mixed by stirring at 4 °C for one day. All formulations are described in detail below in the Results section. Poloxamer 407 (Pluronic® F-127, MW = 12,600 Da), AA (MW = 120,000–190,000 g/mol) and CMC (MW = 700,000 g/mol) were purchased from Sigma (St. Louis, MO, USA); poloxamer 188 (Kolliphor® P-188, MW = 8400 Da) was purchased from BASF (Ludwigshafen am Rhein, Rheinland-Pfalz, Germany); hyaluronic acid (HA, MW = 7000 Da) was obtained from First Chemical (Taipei, Taiwan).
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4

Rifaximin-Based Solid Dispersion Formulation

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Rifaximin (RFX, purity ≥ 98%, molecular weight: 785.9 g/mol, pKa: 6.77) was obtained from Clarochem Ireland Ltd. (Dublin, Ireland). Lacprodan® BLG Pharma Grade (BLG) was obtained from Arla Foods Ingredients (Viby, Denmark). Hydroxypropyl methylcellulose acetate succinate (HPMCAS, AQUAOT®, HF grade) was obtained from Shin-Etsu (Tokyo, Japan). The methacrylic acid-methyl methacrylate co-polymer Eudragit® L100 (EudL) was obtained from Evonik Röhm GmbH (Darmstadt, Germany). Poloxamer 407 (Pluronic® F127) and ammonium formate (≥99.995%) were obtained from Sigma-Aldrich (St. Louis, MO, USA). Methanol (HPLC grade), acetonitrile (HPLC grade), and ethanol (absolute, >99.7%) came from VWR International (Radnor, PA, USA). Water was obtained from a Millipore Milli-Q Ultra Pure water purification system (Billerica, MA, USA).
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5

Ar-Turmerone Loaded Chitosan Gel

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TO containing 12.3% ar-turmerone was purchased from Thai-China Flavours and Fragrances Industry (Nonthaburi, Thailand). Standard ar-turmerone was provided by the Center of Excellence for Innovation in Chemistry, Faculty of Science, Ramkhamhaeng University (Bangkok, Thailand). Chitosan (CS, MW = 63 kDa, 91.74% DD) was supplied by Marine Bio-Resources, Co., Ltd. (Samut Sakorn, Thailand). Sodium Alg (medium viscosity, A2033) and poloxamer 407 (Pluronic® F-127) were purchased from Sigma-Chemicals (St. Louis, MO, USA). FA and N,N’-dicyclohexyl carbodiimide (DCC) were purchased from Tokyo Chemical Industry, Co., Ltd. (Tokyo, Japan). N-hydroxysuccinimide (NHS) was supplied from AK Scientific Inc. (Union City, CA, USA). Dimethyl sulfoxide (DMSO), acetone, and diethyl ether were purchased from Burdick & Jackson Inc. (Muskegon, MI, USA). Acetonitrile was purchased from RCI Labscan Co., Ltd. (Bangkok, Thailand). Triethanolamine was purchased from Merck KGaA (Darmstadt, Germany). Absolute ethanol, glacial acetic acid, calcium chloride (CaCl2), and other chemicals were purchased from Carlo Erba (Val de Reuil, France).
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6

Formulation and Characterization of Nanogel

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β-ST, hyaluronic acid, and Poloxamer 407 (Pluronic F-127) were purchased from Sigma Aldrich, USA. Glyceryl monooleate (GMO) received as a gift from Masterowin Pharmaceuticals, India. Polyvinylpyrrolidone (PVP) –K 30 was purchased from Spectrum Chemical, USA. Methanol and acetonitrile were bought from Merck, India. Distilled water was obtained from an inner source. All other chemicals and reagents used in the study were of analytical grade.
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7

Optimized Topical CLT Formulation

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CLT was purchased from Pol-Aura (Różanowo, Poland). Castor oil was supplied from Microfarm (Zabierzów, Poland). Rapeseed oil was purchased from Bunge Polska Sp. z o.o. (Kruszwica, Poland). In addition, 90% Lactic acid, Poloxamer 188 (Pluronic F-68) was purchased from Pol-Aura (Różanowo, Poland). Poloxamer 407 (Pluronic F-127), poly(ethylene glycol) 200 (PEG200), sorbitan monooleate (Span 80), and polyoxyethylenesorbitan monooleate (Tween 80) were purchased from Sigma-Aldrich (St. Louis, MO, USA or Steinheim, Germany). Propylene glycol was supplied by Firma Chempur (Piekary Śląskie, Poland).
Acetonitrile for HPLC (ACN) was purchased from S.Witko (Łódź, Poland). Acetone, methanol, and potassium phosphate monobasic (KH2PO4) were obtained from Chempur (Piekary Śląskie, Poland). Isopropanol was purchased from Pol-Aura (Różanowo, Poland). Milli-Q water (<0.05 µS/cm), used in batches manufacturing and all experiments, was self-produced from Hydrolab Ultra UV (Hydrolab Sp z o.o., Straszyn, Poland). All the chemicals and reagents used in this study were analytical grade.
Market reference, i.e., 1% CLT cream, MycoHydralin (Bayer Healthcare, Loos, France), was purchased in a local retail pharmacy in France.
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8

Chitosan-based Bioactive Nanoparticles

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Intermediate molecular weight chitosan (MMWC; 75–85% deacetylated, Sigma Aldrich, USA), tripolyphosphate (TPP) (Merck, Darmstadt, Germany), poloxamer 407 (Pluronic F- 127) (Sigma Aldrich, USA), glacial acetic acid (Merck, Darmstadt, Germany), and glycerophosphate disodium salt hydrate (Merck, Darmstadt, Germany), nHA (Sigma Aldrich, USA), and NaF powder (Solarbio®, China) were utilized to prepare the formulation.
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9

Pharmaceutical Compound Characterization

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Miltefosine (C21H46NO4P), Acarbose (C25H43NO18), Amphotericin B (AmpB, C47H73NO17) and Poloxamer 407 (Pluronic® F127) were purchased from Sigma-Aldrich (catalog numbers: 58066-85-6, 56,180-94-0, 1397-89-3 and 16,758, respectively; St. Louis, USA).
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10

Triglyceride Secretion Rate in Ldlr-/- Mice

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After overnight fasting, Ldlr−/− mice fed Western diet without finasteride or the same diet containing 1000 mg/kg of finasteride for 12 weeks were injected with 1,000 mg/kg pluronic F127 poloxamer-407 (Sigma-Aldrich) to inhibit lipoprotein clearance from plasma (22 (link), 30 (link)). Blood samples were collected every hour from the tail for four hours to determine the triglyceride secretion rate using commercially available kits (FUJIFILM Wako Diagnostics). As done in the past (31 (link)), we represented secretion rate as the average of the slope referred to the mice fed Western diet without finasteride.
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