Artificial Liposomes With Internal Docking Site for Protein Delivery.
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| Title: | Artificial Liposomes With Internal Docking Site for Protein Delivery. |
|---|---|
| Authors: | Ryu, Hyeri1 (AUTHOR), Lee, Eun Seong2 (AUTHOR) eslee@catholic.ac.kr |
| Source: | Polymers for Advanced Technologies. Apr2025, Vol. 36 Issue 4, p1-9. 9p. |
| Subjects: | Polymersomes, Signal recognition particle receptor, Molecular docking, Deoxycholic acid, Moieties (Chemistry), Liposomes |
| Abstract: | In this study, we developed a liposomal system incorporating two distinct pH‐responsive polymers to enhance the efficiency of protein delivery. Two pH‐responsive polymers were synthesized by conjugating deoxycholic acid (DOCA) and pH‐sensitive moieties [2,3‐dimethylmaleic anhydride (DMA) or 3‐(diethylamino)propylamine (DEAP)] to hyaluronic acid (HA), resulting in HA conjugates with DOCA and DMA (HDOC‐DMA) and with DOCA and DEAP (HDOC‐DEAP). Liposomes were fabricated using the thin‐film hydration technique with hydrogenated soy phosphatidylcholine (HSPC), HDOC‐DEAP, and HDOC‐DMA. Lysozyme (Lyz) was encapsulated within the liposomes using the extrusion method, followed by the addition of hyaluronidase (HAase) to remove HA or HA conjugates from the outer surface of the liposomes. Meanwhile, the incorporation of HDOC‐DMA and HDOC‐DEAP within the liposomal hydrophilic core and hydrophobic shell facilitated electrostatic interactions between the negatively charged DMA and the positively charged Lyz. This interaction ensured the stable immobilization of Lyz within the liposomal core, leading to the formation of the final formulation, (Lyz/HDOC‐DMA/HDOC‐DEAP)@Lipo. Our experimental results demonstrated that (Lyz/HDOC‐DMA/HDOC‐DEAP)@Lipo significantly enhanced Lyz encapsulation efficiency within the liposomal interior. At pH 6.5, the hydrolysis of DMA (inducing electrostatic repulsion between aminated HA and Lyz) and the protonation of DEAP (destabilizing the liposomal structure) collectively facilitated accelerated Lyz release. This system effectively suppresses passive diffusion of the encapsulated protein at pH 7.4 while promoting targeted protein release in a mildly acidic environment, providing a highly efficient platform for protein. [ABSTRACT FROM AUTHOR] |
| Copyright of Polymers for Advanced Technologies is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
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| Items | – Name: Title Label: Title Group: Ti Data: Artificial Liposomes With Internal Docking Site for Protein Delivery. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ryu%2C+Hyeri%22">Ryu, Hyeri</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lee%2C+Eun+Seong%22">Lee, Eun Seong</searchLink><relatesTo>2</relatesTo> (AUTHOR)<i> eslee@catholic.ac.kr</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Polymers+for+Advanced+Technologies%22">Polymers for Advanced Technologies</searchLink>. Apr2025, Vol. 36 Issue 4, p1-9. 9p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Polymersomes%22">Polymersomes</searchLink><br /><searchLink fieldCode="DE" term="%22Signal+recognition+particle+receptor%22">Signal recognition particle receptor</searchLink><br /><searchLink fieldCode="DE" term="%22Molecular+docking%22">Molecular docking</searchLink><br /><searchLink fieldCode="DE" term="%22Deoxycholic+acid%22">Deoxycholic acid</searchLink><br /><searchLink fieldCode="DE" term="%22Moieties+%28Chemistry%29%22">Moieties (Chemistry)</searchLink><br /><searchLink fieldCode="DE" term="%22Liposomes%22">Liposomes</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: In this study, we developed a liposomal system incorporating two distinct pH‐responsive polymers to enhance the efficiency of protein delivery. Two pH‐responsive polymers were synthesized by conjugating deoxycholic acid (DOCA) and pH‐sensitive moieties [2,3‐dimethylmaleic anhydride (DMA) or 3‐(diethylamino)propylamine (DEAP)] to hyaluronic acid (HA), resulting in HA conjugates with DOCA and DMA (HDOC‐DMA) and with DOCA and DEAP (HDOC‐DEAP). Liposomes were fabricated using the thin‐film hydration technique with hydrogenated soy phosphatidylcholine (HSPC), HDOC‐DEAP, and HDOC‐DMA. Lysozyme (Lyz) was encapsulated within the liposomes using the extrusion method, followed by the addition of hyaluronidase (HAase) to remove HA or HA conjugates from the outer surface of the liposomes. Meanwhile, the incorporation of HDOC‐DMA and HDOC‐DEAP within the liposomal hydrophilic core and hydrophobic shell facilitated electrostatic interactions between the negatively charged DMA and the positively charged Lyz. This interaction ensured the stable immobilization of Lyz within the liposomal core, leading to the formation of the final formulation, (Lyz/HDOC‐DMA/HDOC‐DEAP)@Lipo. Our experimental results demonstrated that (Lyz/HDOC‐DMA/HDOC‐DEAP)@Lipo significantly enhanced Lyz encapsulation efficiency within the liposomal interior. At pH 6.5, the hydrolysis of DMA (inducing electrostatic repulsion between aminated HA and Lyz) and the protonation of DEAP (destabilizing the liposomal structure) collectively facilitated accelerated Lyz release. This system effectively suppresses passive diffusion of the encapsulated protein at pH 7.4 while promoting targeted protein release in a mildly acidic environment, providing a highly efficient platform for protein. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Polymers for Advanced Technologies is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/pat.70186 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 9 StartPage: 1 Subjects: – SubjectFull: Polymersomes Type: general – SubjectFull: Signal recognition particle receptor Type: general – SubjectFull: Molecular docking Type: general – SubjectFull: Deoxycholic acid Type: general – SubjectFull: Moieties (Chemistry) Type: general – SubjectFull: Liposomes Type: general Titles: – TitleFull: Artificial Liposomes With Internal Docking Site for Protein Delivery. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ryu, Hyeri – PersonEntity: Name: NameFull: Lee, Eun Seong IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 04 Text: Apr2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 10427147 Numbering: – Type: volume Value: 36 – Type: issue Value: 4 Titles: – TitleFull: Polymers for Advanced Technologies Type: main |
| ResultId | 1 |
