Use of serratia marcesens bacterial vaccine for preparing drug for treating lung fibrosis
A technology for Serratia marcescens and pulmonary fibrosis, applied in drug combinations, medical raw materials derived from bacteria, respiratory diseases, etc., can solve problems such as unsatisfactory effects and single effect
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Embodiment 1
[0019] Cultivation and collection of Serratia marcescens vaccine:
[0020] The working seeds for production are grown in solid state. After inoculating the working seeds for production in the nutrient agar medium, inoculate for 2 consecutive subcultures, and finally inoculate the slant of the nutrient agar medium in the Koch flask, and culture aerobically at 37°C for 19 hours, no more than 4 generations. During the cultivation, there is no special requirement on the cultivation conditions, whichever is suitable for the growth of the Serratia marcescens vaccine, the pH range is 2-9, and the temperature is 4-40°C. The pH value of this experiment is 6, and the temperature is 20°C. Microscopically inspect each bottle before collection, and discard those contaminated with bacteria. The collected bacterial lawn was placed in sterilized saline for injection, mixed thoroughly, and filtered with four layers of silk cloth. Measured according to the Chinese bacterial turbidity standar...
Embodiment 2
[0023] Get 1000ml of pyrogen-free deionized pure distilled water to dissolve 640mg of Serratia marcescens bacterin, mix evenly, sterilize and configure into 0.64mg / ml injection, bottle to make finished product.
Embodiment 3
[0025] The specific experiments and results are described as follows:
[0026] 1 Materials and methods
[0027] 1.1 Reagents and instruments Bleomycin (Pingyangmycin hydrochloride produced by Tianjin Hebei Pharmaceutical Factory, hereinafter referred to as BLM) was dissolved in normal saline to prepare 5 mg / ml.
[0028] 1.2 Animal grouping and treatment methods 80 healthy SD rats (provided by the Department of Experimental Zoology, Second Military Medical University), male or female, weighing (220±28) g. Among them, 48 rats were randomly divided into groups after intratracheal injection of BLMA55mg / kg at one time. ① Model group (24 rats): 0.3ml of normal saline was instilled into the nasal cavity of each rat from the next day after model preparation; ② Serratia marcescens vaccine group (24 rats): From the next day after model preparation, 0.3ml (0.01mg / kg) of Serratia marcescens vaccine was instilled into the nasal cavity of each rat every day for 28 days; ③Normal control gro...
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