Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Use of CM101 in preparing medicine

A technology of 1.CM101, application, applied in the direction of drug combination, preservation and application of human or animal body, etc.

Inactive Publication Date: 2008-05-28
CG赫勒奎斯特
View PDF2 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Continuous wounding that promotes tumor progression may be a common side effect of surgical interventions associated with cancer treatment

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

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Use of CM101 in preparing medicine
  • Use of CM101 in preparing medicine

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0040] A method for the preparation of GBS toxin is provided in US Patent 5,010,062. Preferably, however, CM101 is purified as taught in International Application PCT / US97 / 17535, incorporated herein by reference.

[0041] The starting material for isolating CM101 used in the method of the present invention can be obtained by culturing strains of Group B β-hemolytic Streptococcus that have recently infected or are capable of infecting newborns. Isolates of this strain can be obtained from the blood or cerebrospinal fluid of infected neonates.

[0042] The GBS toxin used in the present invention is limited to any ingredient or component isolated from native or lysed GBS bacteria, or obtained from the culture supernatant of lysed and / or autoclaved GBS bacteria, and which is induced to breathe in sheep Biological activity confirmed by distress test (Hellerqvist, C.G. et al., Studies on group B beta-hemolytic streptococci I. Isolation and partial identification of extracellular to...

Embodiment 1

[0060] Example 1: CM101 promotes wound healing in tumor-free subjects.

[0061] The effect of CM101 on wound healing was determined in tumor-free CD-1 nude mice. The wound was made with fine surgical scissors and consisted of a 4 mm thick skin incision. with a sterile adhesive bandage (Tegadem Tm , USA) to cover each wound.

[0062] On day 0 of the experiment, mice were intravenously administered 240 μg / kg CM101 or saline and wounded. Neovascularization at each wound site was assessed using magnetic resonance microimaging (MRI), which was performed on days 0, 1, 2, 3, and 5.

[0063] MRI experiments were performed on a horizontal 4.7 T biopsy spectrometer (Bruker, Germany) using a 2 cm surface radiofrequency coil. Gradient echo images (slice thickness 0.5 mm, TR 100 ms, 256×256 pixels, 110 μm plane resolution) were acquired with echo times of 10.5 and 20 ms. Growth in the capillary bed was reflected by a decrease in mean intensity in the 1 mm area around the incision. An...

Embodiment 2

[0065] Example 2: CM101 Promotes Wound Healing in Tumor Subjects.

[0066] The effect of CM101 on wound neovascularization was examined using mice implanted with glioma spheroids. A single C6 glioma spheroid (approximately 800 μm in diameter) was implanted subcutaneously in the lower dorsum of each male CD-1 nude mouse (Abramovitch R., Meir G. and Neeman M., Neovascularization induced by implanted C6 nerve Growth of Glioma Multicellular Spheroids: Magnetic Resonance Microimaging, Cancer Research, 55: 1956-1962 (1995)).

[0067] Eight days later, on day 0 of the experiment, mice were anesthetized by intraperitoneal injection of 75 μg / g ketamine and 3 μg / g xylazine. Mice were injected with saline containing 0, 60, 120 or 240 μg / kg CM101 via the tail vein. Wound site neovascularization was assessed using Magnetic Resonance Imaging (MRI) as described in Example 1. Each anesthetized mouse was placed in the supine position in the MRI equipment and the tumor was located in the cen...

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

No PUM Login to View More

Abstract

The present invention includes a means of treating a patient having a keloid. Specifically, the invention includes a method for excising the keloid and administering a GBS toxin isolated from Group B beta-hemolytic Streptococcus bacteria.

Description

technical field [0001] The present invention relates to promoting wound healing in patients by reducing scarring and accelerating healing. The invention also relates to reducing the development of tumors associated with wounds. Background technique [0002] The normal healing process of skin wounds from surgery or trauma involves blood clots and often scab formation. More specifically, primary or primary healing generally occurs in clean incisions, whereas secondary or secondary healing occurs in wounds with dehiscent edges. Protein fibers fill the skin edges around the wound, and a scab seals the wound and prevents infection. Wound edges re-epithelialize and grow capillaries from blood vessels when the inflammatory response triggers an increase in the number of blood cells in the area that aids in the repair process. Capillaries in the wound area regenerate and participate in the formation of granulation tissue, which in turn contributes to scarring. [0003] Granulatio...

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
Patent Type & Authority Patents(China)
IPC IPC(8): A61K31/715A61K35/74A61P17/02A61P43/00
CPCA61K31/715A01N1/0226A61P17/02A61P43/00
Inventor C·G·赫勒奎斯特M·尼曼B·D·瓦米尔R·阿布拉莫维齐
Owner CG赫勒奎斯特
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products