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Medicine-loaded long-cycle modified nanometer montmorillonite clay material and preparation method thereof

A nano-montmorillonite, long-cycle technology, applied in the field of biomedical materials, can solve the problems of short half-life, insufficient drug loading, large toxic and side effects, etc., and achieve the effects of enhanced adsorption performance, difficult metabolism, and small burst release effect.

Pending Publication Date: 2020-01-17
AFFILIATED HOSPITAL OF NANTONG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Liposomes and micelles entrap anti-tumor drugs to target tumor sites, but there are still many problems, such as short half-life in vivo, insufficient drug loading, and large toxic and side effects.

Method used

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  • Medicine-loaded long-cycle modified nanometer montmorillonite clay material and preparation method thereof
  • Medicine-loaded long-cycle modified nanometer montmorillonite clay material and preparation method thereof
  • Medicine-loaded long-cycle modified nanometer montmorillonite clay material and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] Step 1: Soak montmorillonite K-10 in 50g / L sulfuric acid solution, stir for 2h, then dry, calcinate at 300°C for 4h, then soak in 20g / L sodium polyphosphate solution at 60°C, stir for 12h, then Drying, calcining at 300°C for 4 hours, and then grinding and sieving to obtain activated montmorillonite with a particle size of <120nm;

[0029] Step 2: Dissolve 3 mg of doxorubicin in 300 ml of PBS buffer solution with pH 7.4, mix with 30 mg of activated montmorillonite and 30 mg of graphene, and then spray dry. h prepared drug-loaded montmorillonite;

[0030] Step 3: 3 mg of drug-loaded montmorillonite is activated by plasma treatment. The plasma treatment conditions are as follows: the gas is oxygen, the treatment power is 280 W, the pressure is 55 Pa, and the treatment time is 12 minutes. Under the condition of vacuum degree of 0.024mBar, it was dispersed in 15ml of PBS buffer solution together with 8mg of serine, and freeze-dried at -40°C and 0.020mBar to prepare the drug...

Embodiment 2

[0033] Step 1: Soak montmorillonite K-10 in 50g / L sulfuric acid solution, stir for 2h, then dry, calcinate at 300°C for 4h, then soak in 20g / L sodium polyphosphate solution at 60°C, stir for 12h, then Drying, calcining at 300°C for 4 hours, and then grinding and sieving to obtain activated montmorillonite with a particle size of <120nm;

[0034] Step 2: Dissolve 5 mg of doxorubicin in 100 ml of PBS buffer at pH 7.4, mix with 10 mg of activated montmorillonite and 10 mg of graphene, and then spray dry. h prepared drug-loaded montmorillonite;

[0035] Step 3: 1 mg of drug-loaded montmorillonite is activated by plasma treatment. The plasma treatment conditions are as follows: the gas is nitrogen, the treatment power is 250 W, the pressure is 50 Pa, and the treatment time is 10 minutes. Under the condition of vacuum degree of 0.010mBar, it was dispersed in 5ml of PBS buffer solution together with 2mg of serine, and freeze-dried at -50°C and 0.010mBar to prepare the drug-loaded lo...

Embodiment 3

[0037] Step 1: Soak montmorillonite K-10 in 50g / L sulfuric acid solution, stir for 2h, then dry, calcinate at 300°C for 4h, then soak in 20g / L sodium polyphosphate solution at 60°C, stir for 12h, then Drying, calcining at 300°C for 4 hours, and then grinding and sieving to obtain activated montmorillonite with a particle size of <120nm;

[0038] Step 2: Dissolve 1 mg of paclitaxel in 500 ml of PBS buffer solution with pH 7.4, mix it with 50 mg of activated montmorillonite and 50 mg of graphene, and then spray dry it with an air inlet temperature of 160°C and a feed flow rate of 1 L / h Drug-loaded montmorillonite;

[0039] Step 3: Activate 5 mg of drug-loaded montmorillonite through a plasma processor. The plasma treatment conditions are as follows: the gas is oxygen, the processing power is 300 W, the pressure is 60 Pa, and the processing time is 15 minutes. Under the condition of vacuum degree of 0.060mBar, it was dispersed in 20ml of PBS buffer solution together with 10mg of...

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Abstract

The invention discloses a medicine-loaded long-cycle modified nanometer montmorillonite clay material and a preparation method thereof. The preparation method comprises the steps of sufficiently stirring and soaking montmorillonite clay with a sulfuric acid solution, performing drying, and performing calcinating at 250-350 DEG C for 3-5h; performing sufficient stirring and soaking with a sodium hexametaphosphate solution at 50-65 DEG C, performing drying, and performing calcinating at 250-350 DEG C for 3-5h; performing grinding and screening to obtain activated montmorillonite clay of which the particle size is smaller than 120nm; enabling antitumor drugs to dissolve in a PBS buffer solution to obtain a mixture, mixing the mixture with the activated montmorillonite clay and the graphene, and performing spray drying to obtain the medicine-loaded montmorillonite clay; treating and activating the prepared medicine-loaded montmorillonite clay with a plasma processor, performing dispersingwith serine under the vacuum condition in the PBS buffer solution, and performing freeze drying to obtain the medicine-loaded long-cycle modified nanometer montmorillonite clay material.

Description

technical field [0001] The invention belongs to the field of biomedical materials, in particular to a drug-loaded long-cycle modified nano-montmorillonite material and a preparation method thereof. Background technique [0002] Macromolecular drugs, including liposomes, cannot enter normal tissues through blood vessels, but increase their accumulation in tumor tissues and prolong their retention time. This phenomenon is called the EPR effect. Taking advantage of this effect, at present, people have developed a variety of pharmaceutical preparations for treating tumors, mainly including liposomes and various types of micelles. Liposomes and micelles entrap anti-tumor drugs to target tumor sites, but there are still many problems, such as short half-life in vivo, insufficient drug loading, and large toxic and side effects. Contents of the invention [0003] Purpose of the invention: The technical problem to be solved by the present invention is to provide a long-cycle drug-...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A61K47/52A61K31/704A61K31/337A61P35/00
CPCA61K47/52A61K31/704A61K31/337A61P35/00
Inventor 陆舒尹晓敏赵宏胜王林华
Owner AFFILIATED HOSPITAL OF NANTONG UNIV