Pickering emulsion and drug-loaded emulsion with temperature-controlled release behavior and preparation method
An emulsion and drug-carrying technology, which is applied to medical preparations with non-active ingredients, medical preparations containing active ingredients, and pharmaceutical formulas, can solve problems such as high cost, damage to biological cells, and stimulation of biological tissues. Mild reaction conditions, easy particle recovery, and short reaction time
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Embodiment 1
[0064] Weigh 25 mg of SiO 2 @short-PNIPAm-I particles, disperse them in 5mL deionized water, place them in an ultrasonic cleaner for about 5min in an ice-water bath until the particles are evenly dispersed, then add 5mL isopropyl myristate as the oil phase, Stir with a homogeneous stirrer for 5min (18000r / min) under the condition of ice-water bath. That is, the obtained W / O type Pickering emulsion.
Embodiment 2
[0066] Weigh 25 mg of SiO 2@short-PNIPAm-II particles, disperse them in 5mL deionized water, place them in an ultrasonic cleaner for about 5min in an ice-water bath until the particles are evenly dispersed, then add 6mL isopropyl myristate as the oil phase, Stir with a homogeneous stirrer for 5min (16000r / min) under the condition of ice-water bath. That is, the obtained W / O Pickering emulsion.
Embodiment 3
[0068] Weigh 25 mg of SiO 2 @medium-PNIPAm particles, disperse them in 5mL deionized water, place them in an ultrasonic cleaner for about 5min in an ice-water bath until the particles are uniformly dispersed, add 5mL trichlorethylene as the oil phase, and use them in an ice-water bath Stir with a homogeneous mixer for 5min (18000r / min). That is, the obtained O / W type Pickering emulsion.
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