A gum Arabic assisted sustainable drug delivery system for adult Drosophila
Journal: 2020/June - Biology Open
Abstract:
Large-scale compound screening in adult flies is hampered by the lack of continuous drug delivery systems and poor solubility of numerous compounds. Here we found that gum Arabic (Acacia/Senegal gum), a widely used stabilizer, can also emulsify lipophilic compounds and profoundly increase their accessibility to target tissues in Drosophila and mice. We further developed a gum Arabic-based drug delivery system, wherein the drug was ground into gum Arabic and emulsified in liquid food fed to flies by siphoning through a U-shape glass capillary. This system did not affect food intake nor cell viability. Since drugs were continuously delivered by siphoning, minimal compound waste and less frequent food changes make this system ideal for large-scale long-term screenings. In our pilot screening for antitumor drugs in the NCI DTP library, we used a Drosophila model of colorectal cancer and identified two drugs that are especially hydrophobic and were not identified in previous screenings. Our data demonstrated that gum Arabic facilitates drug delivery in animal models and the system is suitable for long-term high-throughput drug screening in Drosophila This system would accelerate drug discovery for chronic and cognitive conditions.
Keywords: Compound screen; Drosophila; Drug delivery; Gum Arabic.
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Biol Open 9(6): bio052241

A gum Arabic assisted sustainable drug delivery system for adult <em>Drosophila</em>

Shanghai East Hospital, School of Life Sciences and Technology, Tongji University, 6B, Shixun Building, 1239 Siping Road, Yangpu District, 20092, China
College of Animal Sciences and Technology, Guangxi University, Nanning, 530004, China
These authors contributed equally to this work
Author for correspondence (nc.ude.ijgnot@gnedh)
Received 2020 Mar 18; Accepted 2020 May 11.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

ABSTRACT

Large-scale compound screening in adult flies is hampered by the lack of continuous drug delivery systems and poor solubility of numerous compounds. Here we found that gum Arabic (Acacia/Senegal gum), a widely used stabilizer, can also emulsify lipophilic compounds and profoundly increase their accessibility to target tissues in Drosophila and mice. We further developed a gum Arabic-based drug delivery system, wherein the drug was ground into gum Arabic and emulsified in liquid food fed to flies by siphoning through a U-shape glass capillary. This system did not affect food intake nor cell viability. Since drugs were continuously delivered by siphoning, minimal compound waste and less frequent food changes make this system ideal for large-scale long-term screenings. In our pilot screening for antitumor drugs in the NCI DTP library, we used a Drosophila model of colorectal cancer and identified two drugs that are especially hydrophobic and were not identified in previous screenings. Our data demonstrated that gum Arabic facilitates drug delivery in animal models and the system is suitable for long-term high-throughput drug screening in Drosophila. This system would accelerate drug discovery for chronic and cognitive conditions.

KEY WORDS: Gum Arabic, Drug delivery, Compound screen, Drosophila

Acknowledgements

We thank Bloomington Drosophila Stock Center and Dr Henri Jasper for fly stocks.

Footnotes

Competing interests

A provisional patent application related to this work has been filed by Tongji University.

Author contributions

Conceptualization: P.M., H.D.; Methodology: Q.L., P.M., Q.Z., Y.Y.; Validation: Q.L., P.M., Q.Z., P.W., H.D.; Formal analysis: Q.L., Y.Y., P.W., Y.Z.; Investigation: Q.L., P.M., Y.Y., P.W., S.W., Y.Z., R.H.; Writing - original draft: H.D.; Writing - review &amp; editing: H.D.; Visualization: Q.L., S.W.; Supervision: S.W., H.D.; Project administration: H.D.; Funding acquisition: H.D.

Funding

This work was supported by a National Key Research and Development Project [2018YFA0107100], National Natural Science Foundation of China [grant no. 31871371] and Tongji University Basic Scientific Research-Interdisciplinary Fund [grant no. 2000123424] to H.D.

Supplementary information

Supplementary information available online at https://bio.biologists.org/lookup/doi/10.1242/bio.052241.supplemental

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