摘要:
A jelly preparation containing biguanide medicine that at administration, suppresses bitterness and harsh taste and reduces discomfort, and that despite having stability, excels in medicine release in the gastrointestinal tract. There is provided a jelly preparation containing biguanide medicine characterized in that a biguanide medicine, an inorganic acid and a water soluble polymer are contained. By virtue of the particular action of the inorganic acid, the conflicting properties of excelling in jelly preparation stability and medicine release can be simultaneously realized.
摘要:
A microneedle and a microneedle array which can support not only a drug but also a stabilizer and a thickener in large quantities and have excellent puncture property. The microneedle is used to administer a drug transdermally and comprises a top section, a shaft section and a base section, wherein (i) the tip apex angle (±) is 15 to 60°; (ii) the tip diameter (D 0 ) is 1 to 20 µm; (iii) the area (A 3 ) of the top surface of the base section is larger than the area (A 2 ) of the bottom surface of the shaft section; (iv) the following expressions (1) and (2) are satisfied H / D 4 ‰§ 3 (H is the overall height, and D 4 is the diameter of the bottom surface of the base section) ² ‰§ 90 - 0.5 �¢ ± (² is the angle formed between the side surface of the shaft section and the top surface of the base section, and ± is the tip apex angle.); and (v) a solid composition containing a drug is fixed to the side surface of the shaft section and the following expression (5) is satisfied. 10 �¢ ° ‰¦ ³ ‰¦ 60 �¢ ° (³ is the angle formed by tangent lines connecting the apex of the top section and the surface of the solid composition fixed to the side surface of the shaft section.)
摘要:
In the conventional micropatch method, the skin is pricked with solid needles, and vibration is applied by means of a vibrator so as to increase the needle-skin interstice to thereby accomplish drug administration. In the invention, there are provided a pad base for transdermal drug administration whereby transdermal administration of a medicinal drug can be accomplished without need to apply vibration, and provided a process wherein the pad base can easily be produced. One end of each of metal thin wires is immersed in the vertical direction in a synthetic resin raw material solution so as to cause the synthetic resin raw material solution to adhere to the circumference of the metal thin wires. The synthetic resin raw material solution is hardened, and thereafter the metal thin wires are pulled out. Thus, there can be obtained a structure comprising adherent substrate (2) and, disposed erect on the skin side surface thereof, microneedles (1) being tubular and having bell-bottom outer wall. Medicinal drug charged in the hollow portion (3) of microneedles (1) can be injected in the skin, thereby effecting transdermal drug administration. Further, the microneedles (1) are resistant to breaking off because of the bell-bottom shaping.
摘要:
An anti-inflammatory analgesic for external use containing etodolac as NSAID, which is excellent not only in skin permeability but also in the penetration into tissues present in the portions deeper than the skin and the diffusion in the tissues and which can act directly on the muscles or joint tissues with inflammation or pain and is little irritant to the skin, more specifically, an anti-inflammatory analgesic characterized by containing etodolac and a local anesthetic.