利用立体光刻技术轻松制作可降解的锯齿状聚乙烯二丙烯酸酯微针。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmaceutical Development and Technology Pub Date : 2024-11-01 Epub Date: 2024-10-10 DOI:10.1080/10837450.2024.2413146
Vedant Joshi, Nidhi Singh, Pallab Datta
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引用次数: 0

摘要

微针具有微创给药的潜力。然而,由于缺乏快速、可扩展的制造方法,微针在制造复杂阵列和锯齿以增强粘附性方面受到限制。立体光刻(SLA)等 3D 打印技术是快速、可扩展的方法,但 SLA 需要不可降解的硬质树脂。这项研究试图利用聚(乙二醇二丙烯酸酯)(PEGDA,F3)树脂来克服这一限制,并展示了它与商用 SLA 打印机的兼容性。FESEM 图像显示,使用 SLA 3D 打印机打印定制生物墨水(F3)的效率很高,与商用树脂类似。整个 MNA 的机械耐力测试表明,用 F3 树脂打印的 MNs 阵列(485 ± 5.73 N)所需的力大大小于商用 F1 树脂(880 ± 32.4 N)。F1 和 F3 的穿透性能分别为 10.8 ± 2.06 N 和 0.705 ± 0.03 N。在 PBS 中进行的体外降解研究表明,用 F3 树脂制造的 MN 在 7 天后出现降解,而制造商提供的商用 F1 树脂则没有出现降解。猪皮肤组织学检查显示,猪皮肤上形成了三角形孔隙,孔隙长度为 548 μm,并能有效渗透到真皮深层。总之,与商用树脂相比,PEGDA 可用于制造可降解的锯齿状固体 MN。
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Facile fabrication of degradable, serrated polyethylene diacrylate microneedles using stereolithography.

Microneedles have the potential for minimally invasive drug delivery. However, they are constrained by absence of rapid, scalable fabrication methods to produce intricate arrays and serrations for enhanced adhesion. 3D printing techniques like stereolithography (SLA) are fast, scalable modalities but SLAs require non-degradable and stiff resins. This work attempts to overcome this limitation by utilizing a poly (ethylene glycol diacrylate) (PEGDA, F3) resin and demonstrating its compatibility with a commercial SLA printer. FESEM images showed high printing efficiency of customized bioinks (F3) similar to commercial resins using SLA 3D printer. Mechanical endurance tests of whole MNA showed that MNs array printed from F3 resin (485 ± 5.73 N) required considerably less force than commercial F1 resin (880 ± 32.4 N). Penetration performance of F1 and F3 was found to be 10.8 ± 2.06 N and 0.705 ± 0.03 N. In-vitro degradation study in PBS showed that MNs fabricated from F3 resin exhibited degradation after 7 days, which was not observed with the commercial F1 resin provided by the manufacturer. The histology of porcine skin exhibited formation of triangular pores with pore length of 548 μm and efficient penetration into the deeper dermal layer. In conclusion, PEGDA can be used as for fabricating degradable, serrated solid MNs over commercial resin.

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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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