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Mini 290

Manufactured by Büchi

The Mini-290 is a compact laboratory equipment designed for sample preparation. It features a rotary evaporator function for solvent removal and concentration of liquid samples.

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3 protocols using mini 290

1

Spray-Dried Lipid-Polymer Nanoparticles

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(Note: the following describes 300 ml scale processing). API stock solutions of LPV or 4:1 LPV/RTV (200 mg ml−1 in dichloromethane), polymer (P) PVA (grade 4–88, MW 57–77,000; 50 mg ml−1 in water) and surfactant (S) Kolliphor TPGS (50 mg ml−1 in water) were prepared using standard techniques. Three stock solutions were mixed in the API:P:S ratio 60:192:48 (ml) in a 1:4 dichloromethane to water mixture. Emulsified was conducted using a Hielscher UP400S ultrasonic processor equipped with H14 Probe at 100% output (140 W) for 300 s, with immediate spray-drying using a benchtop spray-dryer (BUCHI Mini-290) with an air-atomizing nozzle and compressed air as the drying gas. Spray-drying process conditions: 7 ml min−1 solution flow rate; 65 °C outlet temperature; and 110 °C inlet temperature. Resultant powders were dried under vacuum for 48 h.
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2

Preparation of LPV SDNs via Emulsion-Spray-Drying

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The LPV SDNs were prepared by emulsion-spray-drying as described by Owen et al. 49 Briefly, a stock solution of LPV (200 mg mL -1 in dichloromethane (DCM)), polyvinyl alcohol (PVA grade 4-88, MW 57-77 000) (50 mg mL -1 in water), Kolliphor TPGS (50 mg mL -1 in water) were prepared. Three stock solutions were mixed in the LPV : PVA : Kolliphor TPGS ratio of 60 : 192 : 48 (mL) in a 1 : 4 DCM to water mixture. Emulsification was conducted using a Hielscher UP400S ultrasonic processor equipped with a H14 Probe at 100% output (140 W) for 180 seconds, with immediate spray-drying using a benchtop spray-dryer (BUCHI Mini-290) with an air-atomizing nozzle and compressed air as the drying gas. Spray-drying process conditions: 7 mL min -1 solution flow rate; 65 °C outlet temperature; 110 °C inlet temperature. Resultant powders were further dried under vacuum for 48 hours to remove residual DCM. SDN dispersions result from subsequent powder dispersion in water; for DLS characterisation, powders were dispersed in distilled water at 2 mg mL -1 (1 mg mL -1 cf. LPV).
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3

Emulsion-Spray-Dried LPV SDNs

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The LPV SDNs were prepared by emulsion-spray-drying as described by Giardiello et al. 22 Briefly, a stock solution of LPV (200 mg mL À1 in dichloromethane (DCM)), polyvinyl alcohol (PVA grade 4-88, M W 57-77 000) (50 mg mL À1 in water), Kolliphor TPGS (50 mg mL À1 in water) were prepared. Three stock solutions were mixed in the LPV : PVA : Kolliphor TPGS ratio of 60 : 192 : 48 (mL) in a 1 : 4 DCM to water mixture. Emulsification was conducted using a Hielscher UP400S ultrasonic processor equipped with a H14 Probe at 100% output (140 W) for 180 seconds, with immediate spray-drying using a benchtop spray-dryer (BUCHI Mini-290) with an air-atomizing nozzle and compressed air as the drying gas. Spray-drying process conditions: 7 mL min À1 solution flow rate; 65 1C outlet temperature; 110 1C inlet temperature. Resultant powders were further dried under vacuum for 48 hours to remove residual DCM. SDN dispersions result from subsequent powder dispersion in water; for DLS characterisation, powders were dispersed in distilled water at 2 mg mL À1 (1 mg mL À1 cf. LPV). The LPV SDNs had a Z-average diameter of 330 nm and PdI of 0.18.
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