Acute Toxicity, Nasal Mucosa Stimulation and Enhancement of Immune Function of Huaxi Guangyi No.1

Ning YANG , Yi LI , Cheng PENG , Ming ZHANG , Xiao-fang XIE

Science Technology and Engineering ›› 2024, Vol. 24 ›› Issue (10) : 4020 -4027.

PDF
Science Technology and Engineering ›› 2024, Vol. 24 ›› Issue (10) : 4020-4027 DOI: 10.12404/j.issn.1671-1815.2305290
research-article
Acute Toxicity, Nasal Mucosa Stimulation and Enhancement of Immune Function of Huaxi Guangyi No.1
Author information +
History +
PDF

Abstract

In order to evaluate the safety and efficacy of the hospital atomization preparation Huaxi Guangyi No.1 to be developed, the safety of Guangyi No.1 was used to investigate by acute toxicity test in mice and nasal mucosa irritation test in rat. The efficacy of Guangyi No.1 was used to investigate by pharmacodynamic test for enhancing immune function. The results show that there is no obvious acute toxicity to mice when 0.34 g/mL of the drug solution was given by atomization within 24 hours. There was no obvious irritation of intranasal administration in rats. Aerosolized administration at 0.068 g/mL tended to increase the thymic index of young mice. It can increase the carbon clearance index K and correction index α of macrophages and the levels of WBC and HGB in peripheral blood of immunocompromised mice induced by cyclophosphamide, and increase the value of hemolysin. It is concluded that the maximum dose of Huaxi Guangyi No.1 aerosol administration in mice is 34 g/kg, and there is no obvious irritation of nasal mucosa. The 0.068 g/mL aerosol administration can enhance immune function and can be used to prevent upper respiratory tract infection.

Cite this article

Download citation ▾
Ning YANG, Yi LI, Cheng PENG, Ming ZHANG, Xiao-fang XIE. Acute Toxicity, Nasal Mucosa Stimulation and Enhancement of Immune Function of Huaxi Guangyi No.1. Science Technology and Engineering, 2024, 24(10): 4020-4027 DOI:10.12404/j.issn.1671-1815.2305290

登录浏览全文

4963

注册一个新账户 忘记密码

References

Funding

PDF (1797KB)

16

Accesses

0

Citation

Detail

Sections
Recommended

/

〈 〉