Octreotide acetate injection drug composition and application thereof

A technology of octreotide acetate and octreotide, which is applied in the field of medicine and can solve problems such as long half-life

Active Publication Date: 2019-03-08
CHENGDU TIANTAISHAN PHARMA
View PDF21 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0008] (2) Long half-life: the half-life of subcutaneous injection is 2 hours

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0108] Embodiment 1: the preparation of octreotide acetate

[0109] 1. Synthetic peptide chain

[0110] (1) Preparation of Boc-Thr(tBu)-OCs

[0111] Take 30.3 g of Boc-Thr(tBu)-OH (FW: 275.3, 110 mmol), dissolve it in 250 ml of methanol and 250 ml of water, pH 2.5. Take another 24g of cesium carbonate (147mmol) and add 100ml of water to dissolve until clear, and slowly add the above-mentioned Boc-Thr(tBu)-OH solution under stirring, and carbon dioxide gas will be generated. The pH of the solution was 7.5. It was dissolved in water at 40-50°C and concentrated to dryness under reduced pressure to obtain 54.2 g of Boc-Thr(tBu)-OCs as a syrupy residue.

[0112] (2) Preparation of Boc-Thr(tBu)-O-resin

[0113] Get 100 grams of chloromethyl resin (100-200 mesh, 1.0mmol / g, 100mmol), soak in DMF for 30 minutes, make the resin fully swell, add step (1) gained syrupy residue 107g and DMF of 700ml, 50- React at 55°C for 48 hours.

[0114] After filtering, the resin was washed twice...

Embodiment 2

[0145] Embodiment 2: the preparation of octreotide acetate

[0146] 1. Synthetic peptide chain

[0147] With embodiment 1.

[0148] Two, disulfide bond ring formation

[0149] Dissolve 90g of the reduced octreotide crude product in 90L of water, slowly add 2M ammonia water dropwise to pH7.8 under stirring, and feed air into the solution at room temperature (the used air passes through saturated calcium hydroxide solution and 2.5M sulfuric acid in advance) solution), so that the disulfide bonds undergo a ring-forming reaction for about 24-36 hours, add glacial acetic acid to adjust the pH to 5.5, add activated carbon to stir for 30 minutes, and filter.

[0150] 3. Separation and purification

[0151] Gained whole filtrate is purified in batches through C18 column when disulfide bonds are formed into rings, mobile phase: 0.25mol / L potassium acetate: acetonitrile (7.2:2.8); Flow rate is: 800ml / min; Effluent, the detection wavelength is: 280nm; after the sample peaks are com...

Embodiment 3

[0152] Embodiment 3: the preparation of octreotide acetate

[0153] 1. Synthetic peptide chain

[0154] With embodiment 1.

[0155] Two, disulfide bond ring formation

[0156] Dissolve 90g of reduced octreotide crude product in 90L of water, slowly add 2M ammonia water dropwise to pH7.8 under stirring, and feed air into the solution at room temperature (the used air passes through 2.5M sulfuric acid solution and saturated calcium hydroxide in advance solution), so that the disulfide bonds undergo a ring-forming reaction for about 24-36 hours, add glacial acetic acid to adjust the pH to 5.5, add activated carbon to stir for 30 minutes, and filter.

[0157] 3. Separation and purification

[0158] Gained whole filtrate is purified in batches through C18 column when disulfide bonds are formed into rings, mobile phase: 0.25mol / L potassium acetate: acetonitrile (7.2:2.8); Flow rate is: 800ml / min; Effluent, the detection wavelength is: 280nm; after the sample peaks are combined...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
Specific rotationaaaaaaaaaa
Login to view more

Abstract

The invention relates to an octreotide acetate injection drug composition and application thereof. The octreotide acetate injection drug composition comprises 0.1g of octreotide acetate (by octreotide), 40-50g of mannitol, 3-4g of lactic acid, an appropriate amount of sodium hydrogen carbonate with the pH adjusted to 3.7-4.7, 1000ml of water for injection, and the like. The invention also discloses an octreotide acetate product and a preparation method thereof. The invention further relates to a method of determining impurities, such as oxidatively degraded impurities, in the octreotide acetate or the composition thereof. The octreotide acetate injection drug composition displays excellent technical effects as described in the description, for example, bulk drugs have higher production efficiency in the preparation process than those in the prior art, the drug loss during injection preparation is significantly reduced, and the growth rate of the impurities in long-term stability reserved samples is significantly lower than that in the prior art.

Description

technical field [0001] The invention belongs to the technical field of medicine. More specifically, the invention discloses a pharmaceutical composition of octreotide acetate injection, octreotide acetate, and a preparation method of the pharmaceutical composition of octreotide acetate injection. The invention also relates to the injection of octreotide acetate Liquid pharmaceutical use. The octreotide acetate injection pharmaceutical composition prepared by the invention and the octreotide acetate have excellent properties. Background technique [0002] Octreotide Acetate (Octreotide Acetate) is a synthetic polypeptide composed of eight amino acids, its chemical name is: D-phenylalanyl-L-cysteinyl-L-phenylalanyl-D-tryptophanyl-L- Lysyl-L-threonyl-N-[(1R,2R)-2-hydroxy-1-(hydroxymethyl)propyl]-L-cysteineamide ring (2→7)-disulfide bond Acetate, its English chemical name is: L-Cysteinamide, D-phenylalanyl-L-cysteinyl-L-phenylalanyl-D- tryptophyl-L-lysyl-L-threonyl-N-[2-hydrox...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): A61K38/08A61K9/08A61K47/26A61K47/12A61P35/00A61P1/00A61P1/18A61P7/04A61P35/04A61P5/00C07K7/06C07K1/04C07K1/06
CPCA61K38/08A61K47/12A61K47/26A61P1/00A61P1/18A61P5/00A61P7/04A61P35/00A61P35/04A61K9/0019A61K9/08C07K7/06Y02P20/55
Inventor 吴国庆张莲莲刘灵刘巧梅吴敏冯敏赵东明
Owner CHENGDU TIANTAISHAN PHARMA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap