Design and construction of three-dimensional physiologically-based vascular branching networks for respiratory assist devices.
Saved in:
| Title: | Design and construction of three-dimensional physiologically-based vascular branching networks for respiratory assist devices. |
|---|---|
| Authors: | Santos, Jose A.1 (AUTHOR), Gimbel, Alla A.1 (AUTHOR), Peppas, Athanasios2 (AUTHOR), Truslow, James G.1 (AUTHOR), Lang, Daniel A.1 (AUTHOR), Sukavaneshvar, Sivaprasad3 (AUTHOR), Solt, Derek3 (AUTHOR), Mulhern, Thomas J.1 (AUTHOR), Markoski, Alex1 (AUTHOR), Kim, Ernest S.1 (AUTHOR), Hsiao, James C.-M.1 (AUTHOR), Lewis, Diana J.1 (AUTHOR), Harjes, Daniel I.1 (AUTHOR), DiBiasio, Christopher1 (AUTHOR), Charest, Joseph L.1 (AUTHOR), Borenstein, Jeffrey T.1 (AUTHOR) jborenstein@draper.com |
| Source: | Lab on a Chip. 12/7/2021, Vol. 21 Issue 23, p4637-4651. 15p. |
| Subjects: | Labs on a chip, Microfluidic devices, Blood flow, Medical equipment, Heart assist devices, Blood pressure, Microfluidics, Acute diseases |
| Abstract: | Microfluidic lab-on-a-chip devices are changing the way that in vitro diagnostics and drug development are conducted, based on the increased precision, miniaturization and efficiency of these systems relative to prior methods. However, the full potential of microfluidics as a platform for therapeutic medical devices such as extracorporeal organ support has not been realized, in part due to limitations in the ability to scale current designs and fabrication techniques toward clinically relevant rates of blood flow. Here we report on a method for designing and fabricating microfluidic devices supporting blood flow rates per layer greater than 10 mL min−1 for respiratory support applications, leveraging advances in precision machining to generate fully three-dimensional physiologically-based branching microchannel networks. The ability of precision machining to create molds with rounded features and smoothly varying channel widths and depths distinguishes the geometry of the microchannel networks described here from all previous reports of microfluidic respiratory assist devices, regarding the ability to mimic vascular blood flow patterns. These devices have been assembled and tested in the laboratory using whole bovine or porcine blood, and in a porcine model to demonstrate efficient gas transfer, blood flow and pressure stability over periods of several hours. This new approach to fabricating and scaling microfluidic devices has the potential to address wide applications in critical care for end-stage organ failure and acute illnesses stemming from respiratory viral infections, traumatic injuries and sepsis. [ABSTRACT FROM AUTHOR] |
| Copyright of Lab on a Chip is the property of Royal Society of Chemistry 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.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: egs DbLabel: Engineering Source An: 153818069 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Design and construction of three-dimensional physiologically-based vascular branching networks for respiratory assist devices. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Santos%2C+Jose+A%2E%22">Santos, Jose A.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Gimbel%2C+Alla+A%2E%22">Gimbel, Alla A.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Peppas%2C+Athanasios%22">Peppas, Athanasios</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Truslow%2C+James+G%2E%22">Truslow, James G.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lang%2C+Daniel+A%2E%22">Lang, Daniel A.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Sukavaneshvar%2C+Sivaprasad%22">Sukavaneshvar, Sivaprasad</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Solt%2C+Derek%22">Solt, Derek</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mulhern%2C+Thomas+J%2E%22">Mulhern, Thomas J.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Markoski%2C+Alex%22">Markoski, Alex</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kim%2C+Ernest+S%2E%22">Kim, Ernest S.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hsiao%2C+James+C%2E-M%2E%22">Hsiao, James C.-M.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lewis%2C+Diana+J%2E%22">Lewis, Diana J.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Harjes%2C+Daniel+I%2E%22">Harjes, Daniel I.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22DiBiasio%2C+Christopher%22">DiBiasio, Christopher</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Charest%2C+Joseph+L%2E%22">Charest, Joseph L.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Borenstein%2C+Jeffrey+T%2E%22">Borenstein, Jeffrey T.</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> jborenstein@draper.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Lab+on+a+Chip%22">Lab on a Chip</searchLink>. 12/7/2021, Vol. 21 Issue 23, p4637-4651. 15p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Labs+on+a+chip%22">Labs on a chip</searchLink><br /><searchLink fieldCode="DE" term="%22Microfluidic+devices%22">Microfluidic devices</searchLink><br /><searchLink fieldCode="DE" term="%22Blood+flow%22">Blood flow</searchLink><br /><searchLink fieldCode="DE" term="%22Medical+equipment%22">Medical equipment</searchLink><br /><searchLink fieldCode="DE" term="%22Heart+assist+devices%22">Heart assist devices</searchLink><br /><searchLink fieldCode="DE" term="%22Blood+pressure%22">Blood pressure</searchLink><br /><searchLink fieldCode="DE" term="%22Microfluidics%22">Microfluidics</searchLink><br /><searchLink fieldCode="DE" term="%22Acute+diseases%22">Acute diseases</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Microfluidic lab-on-a-chip devices are changing the way that in vitro diagnostics and drug development are conducted, based on the increased precision, miniaturization and efficiency of these systems relative to prior methods. However, the full potential of microfluidics as a platform for therapeutic medical devices such as extracorporeal organ support has not been realized, in part due to limitations in the ability to scale current designs and fabrication techniques toward clinically relevant rates of blood flow. Here we report on a method for designing and fabricating microfluidic devices supporting blood flow rates per layer greater than 10 mL min−1 for respiratory support applications, leveraging advances in precision machining to generate fully three-dimensional physiologically-based branching microchannel networks. The ability of precision machining to create molds with rounded features and smoothly varying channel widths and depths distinguishes the geometry of the microchannel networks described here from all previous reports of microfluidic respiratory assist devices, regarding the ability to mimic vascular blood flow patterns. These devices have been assembled and tested in the laboratory using whole bovine or porcine blood, and in a porcine model to demonstrate efficient gas transfer, blood flow and pressure stability over periods of several hours. This new approach to fabricating and scaling microfluidic devices has the potential to address wide applications in critical care for end-stage organ failure and acute illnesses stemming from respiratory viral infections, traumatic injuries and sepsis. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Lab on a Chip is the property of Royal Society of Chemistry 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.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=egs&AN=153818069 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1039/d1lc00287b Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 15 StartPage: 4637 Subjects: – SubjectFull: Labs on a chip Type: general – SubjectFull: Microfluidic devices Type: general – SubjectFull: Blood flow Type: general – SubjectFull: Medical equipment Type: general – SubjectFull: Heart assist devices Type: general – SubjectFull: Blood pressure Type: general – SubjectFull: Microfluidics Type: general – SubjectFull: Acute diseases Type: general Titles: – TitleFull: Design and construction of three-dimensional physiologically-based vascular branching networks for respiratory assist devices. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Santos, Jose A. – PersonEntity: Name: NameFull: Gimbel, Alla A. – PersonEntity: Name: NameFull: Peppas, Athanasios – PersonEntity: Name: NameFull: Truslow, James G. – PersonEntity: Name: NameFull: Lang, Daniel A. – PersonEntity: Name: NameFull: Sukavaneshvar, Sivaprasad – PersonEntity: Name: NameFull: Solt, Derek – PersonEntity: Name: NameFull: Mulhern, Thomas J. – PersonEntity: Name: NameFull: Markoski, Alex – PersonEntity: Name: NameFull: Kim, Ernest S. – PersonEntity: Name: NameFull: Hsiao, James C.-M. – PersonEntity: Name: NameFull: Lewis, Diana J. – PersonEntity: Name: NameFull: Harjes, Daniel I. – PersonEntity: Name: NameFull: DiBiasio, Christopher – PersonEntity: Name: NameFull: Charest, Joseph L. – PersonEntity: Name: NameFull: Borenstein, Jeffrey T. IsPartOfRelationships: – BibEntity: Dates: – D: 07 M: 12 Text: 12/7/2021 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 14730197 Numbering: – Type: volume Value: 21 – Type: issue Value: 23 Titles: – TitleFull: Lab on a Chip Type: main |
| ResultId | 1 |