Thermal Stability of Botulinum Toxin Type A Formulations Exposed to Heat In Vitro, Assessed by an In Vivo Mouse Potency Bioassay.
Abstract
[BACKGROUND] Energy-based devices (EBDs), such as high-intensity focused ultrasound, radiofrequency, and microwave, are increasingly used for facial rejuvenation, raising concerns about whether heat exposure may affect the potency of botulinum toxin.
[OBJECTIVES] This study investigated the thermal stability of 4 commercial botulinum toxin type A (BoNT/A) products under conditions simulating EBD-related heat exposure, which includes 1 liquid formulation (INNOTOX, Medytox, Seoul, South Korea; hereafter referred to as innoBoNT/A) and 3 powder formulations: onabotulinumtoxinA (onaBoNT/A, BOTOX, Allergan, an Abbvie company, North Chicago, IL), incobotulinumtoxinA (incoBoNT/A, XEOMIN, Merz, Frankfurt, Germany), and abobotulinumtoxinA (aboBoNT/A, DYSPORT, Ipsen, Boulogne-Billancourt, France).
[METHODS] Mouse intraperitoneal LD potency assays were performed after exposing reconstituted and liquid formulations to 60°C for 10 to 40 min. Relative and normalized potency values were compared before and after exposure.
[RESULTS] InnoBoNT/A maintained its potency after 25 min of exposure at 60°C, showing no significant loss of biological activity. In contrast, onaBoNT/A, incoBoNT/A, and aboBoNT/A displayed marked reduction in potency under the same conditions. In particular, onaBoNT/A showed a 32% decrease upon exposure at 60°C for 25 min and a complete loss of measurable potency at when exposed at 60°C for 40 min.
[CONCLUSIONS] Among the BoNT/A formulations evaluated, only the liquid-stabilized preparation preserved potency during thermal stress.
[OBJECTIVES] This study investigated the thermal stability of 4 commercial botulinum toxin type A (BoNT/A) products under conditions simulating EBD-related heat exposure, which includes 1 liquid formulation (INNOTOX, Medytox, Seoul, South Korea; hereafter referred to as innoBoNT/A) and 3 powder formulations: onabotulinumtoxinA (onaBoNT/A, BOTOX, Allergan, an Abbvie company, North Chicago, IL), incobotulinumtoxinA (incoBoNT/A, XEOMIN, Merz, Frankfurt, Germany), and abobotulinumtoxinA (aboBoNT/A, DYSPORT, Ipsen, Boulogne-Billancourt, France).
[METHODS] Mouse intraperitoneal LD potency assays were performed after exposing reconstituted and liquid formulations to 60°C for 10 to 40 min. Relative and normalized potency values were compared before and after exposure.
[RESULTS] InnoBoNT/A maintained its potency after 25 min of exposure at 60°C, showing no significant loss of biological activity. In contrast, onaBoNT/A, incoBoNT/A, and aboBoNT/A displayed marked reduction in potency under the same conditions. In particular, onaBoNT/A showed a 32% decrease upon exposure at 60°C for 25 min and a complete loss of measurable potency at when exposed at 60°C for 40 min.
[CONCLUSIONS] Among the BoNT/A formulations evaluated, only the liquid-stabilized preparation preserved potency during thermal stress.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 시술 | botulinum toxin
|
보툴리눔독소 주사 | dict | 3 | |
| 시술 | facial rejuvenation
|
안면거상술 | dict | 1 | |
| 시술 | botox
|
보툴리눔독소 주사 | dict | 1 | |
| 시술 | xeomin
|
보툴리눔독소 주사 | dict | 1 | |
| 시술 | dysport
|
보툴리눔독소 주사 | dict | 1 | |
| 약물 | incobotulinumtoxinA
|
C2930113
incobotulinumtoxinA
|
scispacy | 1 | |
| 약물 | [BACKGROUND] Energy-based
|
scispacy | 1 | ||
| 약물 | [OBJECTIVES]
|
scispacy | 1 | ||
| 약물 | 3 powder formulations
|
scispacy | 1 | ||
| 약물 | onabotulinumtoxinA
|
scispacy | 1 | ||
| 약물 | abobotulinumtoxinA
|
scispacy | 1 | ||
| 약물 | [RESULTS] InnoBoNT/A
|
scispacy | 1 | ||
| 약물 | [CONCLUSIONS]
|
scispacy | 1 | ||
| 질환 | EBDs
→ Energy-based devices
|
scispacy | 1 | ||
| 질환 | INNOTOX
|
scispacy | 1 | ||
| 기타 | Botulinum Toxin Type A Formulations
|
scispacy | 1 | ||
| 기타 | Mouse
|
scispacy | 1 | ||
| 기타 | BoNT/A
→ botulinum toxin type A
|
scispacy | 1 | ||
| 기타 | Merz
|
scispacy | 1 | ||
| 기타 | Ipsen
|
scispacy | 1 | ||
| 기타 | BoNT/A formulations
|
scispacy | 1 |
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