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Paper
보툴리눔 신경 독소의 안전한 제조 방법

CN

ZL 202080059073.1

2024년 8월 6일

재조합 보툴리눔 독소

보툴리눔 신경 독소의 안전한 제조 방법

KR

10-2610179

2023년 11월 30일

재조합 보툴리눔 독소

보툴리늄 독소 전위 도메인 및 엔도라이신을 포함하는 단백질 복합체 및 이를 포함하는 항균 조성물

KR

10-2547393

2023년 6월 20일

재조합 보툴리눔 독소

3분할 단편 생산을 이용한 보툴리눔 신경 독소의 안전한 생산 방법

KR

10-2597062

2023년 10월 27일

재조합 보툴리눔 독소

가용화 파트너 및 GP41.1 인테인을 이용한 보툴리눔 독소 생산방법

KR

10-2731131

2024년 3월 7일

재조합 보툴리눔 독소

FGF 단백질과 BoNT 단백질이 융합된 FGF-BoNT 융합단백질 및 이를 함유하는 화장료 조성물

KR

출원

2024년 10월 24일

재조합 보툴리눔 독소

가용화 파트너 및 인테인을 이용한 보툴리눔 독소 생산방법

KR

출원

2024년 3월 7일

재조합 보툴리눔 독소

보툴리늄 독소 전위 도메인 및 엔도라이신을 포함하는 단백질 복합체 및 이를 포함하는 항균 조성물

US

출원

2023년 10월 17일

재조합 보툴리눔 독소

보툴리눔 신경 독소의 안전한 제조 방법

EU

출원

2022년 2월 22일

재조합 보툴리눔 독소

보툴리눔 신경 독소의 안전한 제조 방법

US

출원

2022년 2월 22일

재조합 보툴리눔 독소

보툴리눔 신경 독소의 안전한 제조 방법

IN

출원

2022년 2월 21일

재조합 보툴리눔 독소

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Recombinant BoNT

Through MVRIX's approach to next-generation botulinum toxins, we have developed recombinant botulinum toxin. From early production stages to diverse applications, we are exploring new possibilities with this differentiated botulinum toxin.

Challenging the Limits of Botulinum Toxin :

Recombinant BoNT

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Solving Strain Issues and Resistance Problems

Pure Toxin Gene for Production in E. coli

MVRIX uses E. coli as the host for botulinum toxin production, eliminating the risk of disputes related to the wild-type Clostridium botulinum strain.

Core Toxin Production to Minimize Resistance

By producing only the pure toxin gene from the initial stages, MVRIX avoids additional purification steps and significantly reduces the risk of resistance.

Expanding Potential Applications

Diverse Botulinum Toxin Types

MVRIX holds multiple serotypes of botulinum toxin and analyzes the unique characteristics of each type and region of action.

New Chimeric Botulinum Toxin Engineering

By engineering different combinations of toxin regions, we expand the versatility, duration, and range of indications for botulinum toxin, pushing the boundaries of its potential applications.

Safe and Fast Production

MVRIX's Two-Part Production Method

MVRIX produces botulinum toxin using E. coli as a host, instead of Clostridium botulinum. Rather than producing the entire core toxin at once, we employ a two-part production method, where the toxin is divided into two non-toxic fragments. These fragments are assembled in the final stage of processing, activating the toxin.

Minimizing Risks, Maximizing Efficiency

Since the toxin remains inactive until the assembly stage, production can be safely conducted at a BSL-2 level.

The entire process, from cultivation to final assembly, takes only one week—one-third of the time required by conventional methods, significantly improving time efficiency.

Core Toxin with Reduced Resistance Risk

Core toxins do not induce resistance to botulinum toxin. With MVRIX’s innovative production method, core toxins can be produced faster and more safely.

Botulinum Toxin with Fast Onset and Long-Lasting Effect

Through protein engineering, MVRIX develops botulinum toxins that act faster and last longer.

Expanding Applications

By engineering each of the three domains of botulinum toxin, MVRIX develops customized toxins for diverse indications.

MVRIX’s recombinant botulinum toxin technology leads the next-generation market with diverse, customized core toxins

What is Botulinum Neurotoxin?

  • Botulinum toxin is a protein toxin produced by the anaerobic bacterium Clostridium Botulinum. It is known as the most potent toxin, with an LD50 (the dose lethal to 50% of test subjects) in mice of 0.0003–0.00003 μg/kg, making it over 30,000 times more potent than the commonly known pufferfish toxin (LD50: 10 μg/kg). Due to its extreme potency, strict safety measures are essential to prevent any release of the strain or toxin into the environment during production and handling.

  • Botulinum toxin consists of three main structural domains.

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  • Botulinum toxin paralyzes muscles by inhibiting the release of neurotransmitters from nerve cells.

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  • Botulinum toxin has seven serotypes (A through G), with types A, B, E, and F being toxic to humans. Each serotype includes around 40 subtypes, and A1 has been the most widely used since its introduction in 1987. Research into various subtypes is ongoing to address resistance issues and meet the therapeutic market demands.

    MVRIX leverages an understanding of the unique characteristics of each serotype and subtype to develop customized botulinum toxins through chimeric manufacturing.

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  • Botulinum toxin produced by Clostridium botulinum is a 900kDa protein complex, with only the 150kDa core toxin responsible for its toxic effects. The remaining 750kDa non-toxic proteins can be recognized as antigens by immune cells, potentially causing resistance. Currently, only three companies globally offer core toxin products with reduced resistance risk.

    MVRIX has developed recombinant technology to produce core toxin through a streamlined process, removing the need for additional purification steps.

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