It suggests that we should take the real-time dissolution test to ensure the intrinsic quality of medicines and drug safety and efficacy.
有必要进行制剂溶出度的实时监测，确保药品的内在质量，保证用药的安全性及有效性。
The USP tablet dissolution test is an analytical tool used for the verification of drug release processes and formulation selection within the pharmaceutical industry.
USP规定的片剂溶出试验被广泛用于医药工业中药物释放过程的验证和处方筛选。
Conclusion: Test of dissolution is helpful for controlling drug quality, and can provide evidence for reasonable clinical administration.
结论：进行溶出度检查有助于控制药品质量，为临床合理用药提供依据。
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