Composition for delivering bioactive material or protein, and use thereof
A bioactive substance and protein technology, applied in the field of delivery of bioactive substance or protein composition, can solve the problems of limited use, difficulty in maintaining protein activity, etc., and achieve the effect of simple cost, no cytotoxicity, and high delivery efficiency
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preparation example Construction
[0125] The preparation method of the porous silica nanoparticles may include a method that is simple and easy to synthesize in large quantities, but is not limited thereto. For example, in the case of using laboratory equipment, at least about 1 g of the porous silica nanoparticles can be produced by the production method once, but the present invention is not limited thereto.
[0126] In an embodiment of the present disclosure, the step of enlarging the pores of the porous silica nanoparticles may include treating the porous silica nanoparticles with tri(C 1-6 Alkyl)benzenes are treated to expand pores, but are not limited thereto. For example, the three (C 1-6 The alkyl)benzene may include trimethylbenzene, triethylbenzene, tripropylbenzene, tributylbenzene, tripentylbenzene, or trihexylbenzene, but is not limited thereto. For example, three (C 1-6 The step of treating alkyl)benzene to expand the pores may include treating the porous silica nanoparticles and tri(C 1-6 Al...
preparation example 1
[0150] Preparation example 1: the synthesis of the porous silica nanoparticle (mesoporous silicanoparticle, MSN) that stomata expands
[0151] The cetyltrimethylammonium bromide (CTAB) of 3.94g and the 1M sodium hydroxide (NaOH) solution of 2.28mL are dissolved in the mixed solution of methanol and water of 800g (methanol: water=0.4:0.6, w / w). Then, while vigorously stirring the obtained solution, 1.3 mL of tetramethoxysilane (TMOS) was added to the solution under atmospheric conditions. After stirring the reaction mixture for 8 hours, it was aged overnight. The obtained white precipitate was subjected to centrifugation to remove the remaining surfactant for purification, and was washed with ethanol and water five times respectively. The porous silica nanoparticles prepared above were suspended in 20 mL of ethanol, and 4 mL of hydrochloric acid was added. Subsequently, the suspension was refluxed overnight to obtain a white powder. The produced white powder was separated ...
preparation example 2
[0153] Preparation example 2: silica nanoparticles (MSNPN) modified with Ni-NTA
[0154] After suspending 100 mg of the pore-enlarged MSN prepared in said Preparation 1 in 10 mL of toluene, 1 mL of 3-aminopropyltriethoxysilane (APTES) was added for amine functionalization. The suspension was refluxed overnight, filtered with a filter, and washed 10 times with ethanol residue to obtain amine-functionalized MSN ( Figure 10a and Figure 10b of 2). 30 mg of the amine-functionalized MSN and 100 mg of 3,3'-dithiodipropionic acid bis(N-hydroxysuccinimide ester) (DTSP) in DMSO were reacted overnight at room temperature. After washing the reaction mixture 3 times with DMSO, add 10 mL of N in DMSO α , N α - Bis(carboxymethyl)-L-lysine hydrate (aminobutyl NTA, 65 mg). The reaction was carried out at room temperature for 24 hours. Then, the NTA-modified MSNs were obtained by washing with ethanol and water 10 times, respectively. In order to Ni 2+ Binding to NTA-modified MSN in 1M...
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