Abstract: A hemostatic material, a preparation method thereof, and a pharmaceutical composition containing the same are introduced. The hemostatic material includes 200 to 1600 parts by weight of water-insoluble gelatin and 100 to 1000 parts by weight of hydrating material. The preparation method for the hemostatic material includes the steps of (a) providing 200 to 1600 parts by weight of water-insoluble gelatin and 100 to 1000 parts by weight of hydrating material; and (b) combining the water-insoluble gelatin with the hydrating material to form a hemostatic material. The pharmaceutical composition includes an aforementioned hemostatic material and active pharmaceutical ingredients. Through the aforementioned hemostatic material, hemostatic products can increase the blood absorption capacity.

Abstract: Nanosilver particles, a porous material composite containing same, and a method of producing same are introduced. The method includes the steps of (a) mixing silver salts-containing precursor and protecting agent to form a first liquid mixture; (b) introducing organic reductant into a first reactant to form a second reactant, wherein the silver salts-containing precursor is reduced by the organic reductant to form nanosilver particles; introducing organic reductant into the first liquid mixture to form a second liquid mixture, wherein the silver salts-containing precursor is reduced by the organic reductant to form nanosilver particles; and (c) introducing alkalinizing agent into the nanosilver particles-containing second liquid mixture. The porous material composite includes a porous material and nanosilver particles attached to outer and inner surfaces of the porous material.

Abstract: A drug carrier, a drug structure, a purpose of the same, a method of making the same, and a method of using the same to inhibit H. pylori are revealed. The drug carrier includes a negatively charged polymer, chitosan and magnetic particles. The purpose of the drug carrier is to make a drug for inhibiting H. pylori. The drug structure includes a negatively charged polymer, chitosan, magnetic particles and an active ingredient. The method of making the drug structure includes mixing the negatively charged polymer solution, the chitosan solution, the magnetic particles and the active ingredient solution to form an initial solution and allowing ingredients in the initial solution to react and thereby form drug structure particles. The method of using the drug structure to inhibit H pylori includes administering the drug structure to an H. pylori colony. The drug carrier and drug structure demonstrate enhanced therapeutic efficacy.

Abstract: A drug carrier carrying an active substance and a method preparing the same are provided. The method includes respectively dissolving a negatively charged polymer, sodium tripolyphosphate, and an active substance in a NaOH aqueous solution to increase the encapsulation rate of the active substance in the drug carrier.

Abstract: A drug carrier, a drug structure, a purpose of the same, a method of making the same, and a method of using the same to inhibit H. pylori are revealed. The drug carrier includes a negatively charged polymer, chitosan and magnetic particles. The purpose of the drug carrier is to make a drug for inhibiting H. pylori. The drug structure includes a negatively charged polymer, chitosan, magnetic particles and an active ingredient. The method of making the drug structure includes mixing the negatively charged polymer solution, the chitosan solution, the magnetic particles and the active ingredient solution to form an initial solution and allowing ingredients in the initial solution to react and thereby form drug structure particles. The method of using the drug structure to inhibit H pylori includes administering the drug structure to an H. pylori colony. The drug carrier and drug structure demonstrate enhanced therapeutic efficacy.

Abstract: A hemostatic material, a preparation method thereof, and a pharmaceutical composition containing the same are introduced. The hemostatic material includes 200 to 1600 parts by weight of water-insoluble gelatin and 100 to 1000 parts by weight of hydrating material. The preparation method for the hemostatic material includes the steps of (a) providing 200 to 1600 parts by weight of water-insoluble gelatin and 100 to 1000 parts by weight of hydrating material; and (b) combining the water-insoluble gelatin with the hydrating material to form a hemostatic material. The pharmaceutical composition includes an aforementioned hemostatic material and active pharmaceutical ingredients. Through the aforementioned hemostatic material, hemostatic products can increase the blood absorption capacity.