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Hot information：
Top 10 Global CDMO Enterprises| The Meaning of IND, NDA and ANDA| Top 10 Global Clinical Research Organizations in 2021
Jan 26,2021
Formulation of Aerosol for Inhalation Administration and Difficulties in Research and Development
Pharmaceutical preparations are drugs that are made in accordance with the requirements of a certain dosage form and can be provided to the subject of medication.
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Formulation of Aerosol for Inhalation Administration and Difficulties in Research and Development
Jan 26,2021
Analysis on the Role of Particle Size Analysis in the Development of Inhalation Preparations
Inhaled medicine refers to a drug delivery method in which the medicine enters the lungs through a special drug delivery device and has a local or systemic effect, thereby achieving the purpose of preventing or treating diseases. In the field of research and development of inhalation preparations, particle size distribution is one of the importantRead more
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Analysis on the Role of Particle Size Analysis in the Development of Inhalation Preparations
Jan 26,2021
The Spray Drying Method of Solid Dispersant Preparation Technology
In the field of drug research, drug candidates are not easily soluble in water, which is one of the challenges that modern drug formulation researchers often face. Due to the low solubility and low bioavailability of this drug, the application of solid dispersion technology can improve the properties of drug compounds that are difficult toRead more
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The Spray Drying Method of Solid Dispersant Preparation Technology
Jan 25,2021
Inventory of Several Sources of Peptide Drugs
Polypeptide is a chemically active substance ubiquitous in organisms. It is a type of compound composed of amino acids connected by peptide bonds. Compared with other chemical drugs and biotechnology drugs, peptide drugs have significant activity, strong specificity, and receptors. The affinity is good, the toxicity is weak, and it is generally not easy toRead more
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Inventory of Several Sources of Peptide Drugs
Jan 25,2021
Analysis on the Advantages of Developing Sustained and Controlled Release Preparations
When developing and designing pharmaceutical preparations, the drugs should be in the best form for diagnosing, treating or preventing human diseases, and the efficacy of the drugs must be maximized and safe. Sustained-release and controlled-release preparations have the advantages of less administration times, less fluctuation in blood concentration, diversified routes of administration, less irritation, long-lastingRead more
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Analysis on the Advantages of Developing Sustained and Controlled Release Preparations
Jan 22,2021
Long-term Drug Stability Test
The stability of drugs is a basic attribute of drugs and one of the important factors for evaluating drug quality. The instability of drugs can lead to increased impurities, decreased bioavailability, decreased safety, increased toxicity, increased side effects and adverse reactions. Therefore, it is necessary to carry out drug stability tests when developing drugs. InRead more
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Long-term Drug Stability Test
Jan 22,2021
Spray Drying Method for Improving the Bioavailability of Poorly Soluble Compounds
In modern formulation research, the preparation of poorly soluble compounds in aqueous media is a difficult problem, and poorly soluble drugs can lead to low drug bioavailability. Solid dispersion is a common method to solve the solubility of poorly soluble drugs, and spray drying is a common technique for preparing solid dispersions. At the beginningRead more
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Spray Drying Method for Improving the Bioavailability of Poorly Soluble Compounds
Jan 22,2021
Lancet Express: Six Months After Jinyintan Patients were Discharged, 76% Still Have Health Effects!
Recently, "The Lancet” published online a cohort study jointly completed by Jinyintan Hospital, China-Japan Friendship Hospital Respiratory Center, National Respiratory Medicine Center, and Institute of Pathogenic Biology, Chinese Academy of Medical Sciences, to evaluate COVID-19 (new coronary pneumonia) ) Long-term effects on patients. Assess the long-term impact of COVID-19 (new coronary pneumonia) on patients TheRead more
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Lancet Express: Six Months After Jinyintan Patients were Discharged, 76% Still Have Health Effects!
Jan 20,2021
Weight difference inspection method of tablet drug analysis technology
Tablets are made by mixing the drug and excipients and then compressed. It is a common oral drug. When analyzing and testing tablet drugs, in order to ensure the uniform quality characteristics of the drug, a weight difference check is required. The uniformity of a drug means that each unit product of a drug preparationRead more
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Jan 20,2021
Analysis on the Function of Clarity Inspection Method in Drug Quality Inspection
Clarity is to check the turbidity of the drug solution, that is, turbidity. The clarity check method is one of the drug impurity analysis methods, mainly to check whether there are insoluble impurities in the drug solution. It can be used as the quality control of the raw material for injection and its injection project.Read more
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