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4 protocols using tetronic 1107

1

Tetronic 1107-Based Biopolymer Synthesis

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Tetronic® 1107 (T1107, molecular mass 15 k Da, HLB:18–23) was donated by BASF Corporation (Florham Park, NJ, USA). Acryloyl chloride, Celite fine 500, 4-dimethylaminopyridine (DMAP), succinic anhydride, N-hydroxysuccinimide (NHS), 4-methoxyphenol (99%), calcium hydride, tetrahydrofuran (THS) and chloroform were purchased from Sigma-Aldrich (St. Louis, MO, USA). Toluene (HPLC grade), diethyl ether (anhydrous, BHT stabilized), and anhydrous sodium sulfate were purchased from Fisher Scientific (Fair Lawn, NJ, USA). Dichloromethane (DCM) (HPLC grade), triethylamine (TEA), ditiothreitol (DTT), sodium bicarbonate, calcium hydride and d-chloroform (CDCl3) were purchased from Acros Organics (Pittsburg, PA, USA) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC) from Tokyo Chemical Industry (Tokyo, Japan). Unless otherwise specified, all chemicals were of analytical grade and were used as received. Double-deionized ultra-filtered water was used throughout this study.
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2

Surface-Modified BaTiO3 Nanoparticle Preparation

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Materials. Tetronic 1107 (T1107) was a gift from BASF, with a reported composition per arm of 60 EO and 20 PO, HLB 18-23 and average molecular weight 15,000 gmol -1 . Inorganic nanoparticles of barium titanate (BT, BaTiO 3 ), with an average diameter of 200 nm were supplied by Nanostructured and Amorphous Materials Inc.
(tetragonal crystalline structure, 99.9% purity, ρ = 6.02 g•cm -3 ), while nanoparticles of 50 nm in diameter were supplied by Sigma-Aldrich (cubic crystalline structure, 99.9% purity, ρ = 6.08 g•cm -3 ).
Preparation of BaTiO 3 nanoparticles. BT nanoparticles present strong aggregation that leads to rapid precipitation in water. Surface modification of the NPs with βcyclodextrin (CD) was performed to overcome this problem, according to the twostep procedure described in a previous work, 39 consisting in the generation of hydroxyl groups on the surface by reaction with H 2 O 2 , followed by mixing with a 10 mM β-CD solution under vigorous stirring. The resulting nanoparticles are centrifuged and washed three times to remove reagents in excess and freeze-dried for storage.
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3

Doxorubicin Delivery System Development

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Doxorubicin hydrochloride (99.9%) was purchased from LKM Laboratories (Argentina). Pluronic ® F127 (F127, MW ∼12.6 kDa, 70 wt % PEO), Tetronic ® 1107 (T1107, MW ∼15.0 kDa, 70 wt% PEO) and Soluplus ® (MW ∼ 120 KDa) were a gift of BASF (Argentina). TPGS (MW ∼1513 g/mol) was purchased from Eastman Chemical Company (USA), sodium deoxycholate (NaDC) was purchased from Riedel-de Häen ® (Germany). Doxil ® was purchased from Raffo Laboratories (Argentina). Tetrazolium compound [3-(4,5-dimethylthiazol-2-yl)-5-(3carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H tetrazolium], inner salt (MTS) and phenazinemethosulfate (PMS) were purchased from Promega Corporation (USA). All solvents were analytical or high performance liquid chromatography (HPLC) grade and were used following the manufacturer's instructions.
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4

Formulation and Characterization of Doxorubicin-Loaded Micelles

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Tetronic ® 1107 (T1107, MW ∼15.0 kDa, 70 wt% PEO) was a gift of BASF ® (Argentina). TPGS (MW ∼1513 g/mol) was purchased from Eastman Chemical Company (USA), sodium deoxycholate (NaDC) was purchased from Riedel-de Häen ® (Germany). Doxorubicin hydrochloride (99.9%) was purchased from LKM Laboratories (Argentina). Doxil ® was purchased from Raffo Laboratories (Argentina). Sodium carboxymethylcellulose was from Fluka-BioChemika (Sigma-Aldrich, Argentina) and sucrose from Anedra (Buenos Aires, Argentina).
Agar-agar was from Laboratorios Britania S.A. (Buenos Aires, Argentina). All other reagents used were from analytical grade.
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