As an effective means of local drug delivery, intratympanic administration has shown a wide range of applications in the treatment of inner ear diseases, such as Meniere's disease, sudden deafness, and immune-related inner ear disease. These diseases have complex etiologies and limited treatment effects, leading to many difficulties in clinical diagnosis and treatment. Intratympanic administration significantly enhances the therapeutic effect through bypassing the blood-labyrinth barrier and increasing the local concentration of the drug in the inner ear. This article reviews the historical development, mechanism and technical advantages of intratympanic administration, and analyzes the application effects of glucocorticoids, gentamicin and other drugs in the treatment of inner ear diseases. At the same time, the limitations and challenges of intratympanic administration in terms of drug absorption, bioavailability, individualized dose control and long-term efficacy were discussed. In the future, with the advancement of nanotechnology and precision medicine, intratympanic administration is expected to achieve higher precision and safety in the treatment of inner ear diseases, providing patients with more optimized treatment options.
Humans ; Labyrinth Diseases/drug therapy* ; Injection, Intratympanic

This study is to explore that how to use the information management system to research composed of the management and sharing of research projects,study exchanging and technical guidance.The purpose is to improve the management efficiency and level of scientific research projects.Current study aimed to explore establish a digital management system

AIM:To construct eukaryotic expression vector expressing double shRNA sections targeting Survivin gene.METHODS: Eukaryotic expression vector expressing double shRNA sections targeting Survivin gene were designed and chemically synthesized.They were directionally inserted into plasmid pGenesil-1 with respectively U6 promoter and termination code,the common green fluorescence protein(EGFP) gene and Neo gene. In this way,the vector of pGenesil-1 shRNA containing 2 sections of Survivin shRNA were constructed and they were transfected into the pancreatic cancer cell Bx-PC3.Transfection was detected by fluorescence microscope.The inhibition expression of Survivin mRNA was measured by RT-PCR.RESULTS: HE1 and HE2 plasmids were identified by the biocatalyst cut which confirmed the exactitude and were analyzed by the sequence analysis which verified the perfect clone plasmid inserted by them.CONCLUSION: A eukaryotic expression vector of double short hairpin RNA for Survivin gene is successfully constructed.The pancreatic cancer cells Bx-PC3 succeed to be transfected and expression of Survivin mRNA is inhibited obviously.