Mesoporous/hollow silica nanocarrier delivery system for targeted activation of CD44 molecules, its preparation method and use
A technology of nano-carrier and delivery system, which can be used in preparations for in vivo tests, non-active components of polymer compounds, nano-drugs, etc., and can solve problems such as non-existence
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[0122] The present invention will be further illustrated by specific examples below, however, it should be understood that these examples are only used for more detailed description, and should not be construed as limiting the present invention in any form.
[0123] This section provides a general description of the materials and test methods used in the tests of the present invention. While many of the materials and methods of manipulation which are employed for the purposes of the invention are well known in the art, the invention has been described here in as much detail as possible. It will be apparent to those skilled in the art that, in the context and context, the materials used and methods of operation used in the present invention are known in the art unless otherwise indicated.
Embodiment 1
[0124] Example 1 Hyaluronic acid (HA) modified loaded rosuvastatin (R) mesoporous silica nanocarrier (mSiO 2 - Preparation of (R)-HA)
[0125] Mesoporous / hollow nanosilicon spheres are made of SiO 2 Nanoparticles composed of materials with mesoporous or hollow structures. The mesoporous / hollow structure can be used to load hydrophilic, hydrophobic or amphiphilic drug molecules, and various targeted enrichment and microenvironmental stimulus-responsive drug release can be achieved by designing its outer surface. This patent selects mesoporous nano-silica spheres (mSiO 2 NPs) are drug carriers, loaded with the therapeutic drug rosuvastatin, and linked with hyaluronic acid (HA) targeting molecules on their surface to achieve targeted recognition and drug delivery.
[0126] 1.1 Mesoporous silica nanocarriers (mSiO 2 NPs) preparation
[0127]Reference Methods Synthesis of Hollow Mesoporous Silica Nanoparticles with Very Large Pores for Enhanced Adsorption and Release of DNA....
Embodiment 2
[0131] Example 2 selectin (SP) modified loaded rosuvastatin (R) mesoporous silica nanocarrier (mSiO 2 - Preparation of (R)-SP)
[0132] Prepare mSiO by a kind of method of embodiment 1 2 Nanocarriers, 1mg mL -1 Rosuvastatin (R)DMSO solution was added dropwise to mSiO 2 NP solution (10mg mL -1 PBS, pH=7.4), after ultrasonication for 30 minutes to mix evenly, stir at room temperature for 24 hours. The nano-drug carriers were precipitated by centrifugation, the supernatant was removed and the pellet was lyophilized to obtain mSiO 2 -(R) nano drug carrier.
[0133] Fully dissolve 1mg of selectin (SP) in PBS buffer solution, add 0.5mg of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC.HCl) and 0.5mg of N - Hydroxysulfosuccinimide (sulfo-NHS) coupling reagent activates the carboxyl group. After stirring the reaction at room temperature for 1 hour, the unreacted small organic molecules were purified by ultrafiltration. Prepare the activated SP to 1 mg mL -1...
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