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The influence of sugar molecule type on the stability of lyophilized human serum albumin (HSA) nanocolloid kit

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Abstract

Using sugar molecules as lyophilization protectants in HSA nanocolloid kit formulations is critical to obtaining kits with excellent stability. A thermal gelation method with no sugar treatment and variations in sugar (glucose, maltose, and lactose) was applied to produce these kits. The particle size and radiochemical purity results showed that HSA nanocolloid kits with sugar excipients are more stable than those without sugar. The addition of lactose as an excipient (HSA: lactose 1:10) results in a stable nanocolloid system, allowing for the development of novel lyophilized HSA nanocolloid kit formulations.

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Acknowledgements

The present study was supported by The National Research and Innovation Agency (BRIN) under the Research and Innovation Program for Advanced Indonesia (decree number 82/II.7/HK/2022) and The Indonesian Endowment Funds for Education (LPDP). The authors are grateful to Ms. Grace Tjungirai Sulungbudi and Ms. Mujamilah (Research Center for Radiation Detection and Nuclear Analysis Technology) for their continued support of this project.

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All authors contributed equally to this work. RDH: designed the study, wrote the manuscript, conducted experiments, supervised the work, WL: methodology, performed experiments, funding acquisition, project administration, SJ: the main conceptual ideas, editing, analyzed the data, conducted the experiments, VYS: performed experiments, funding acquisition, ARP: visualization, data curation, performed experiments, AF: visualization, data curation, performed experiments, LDP: processed the experimental data, performed the analysis, conducted experiments, SS: methodology, performed experiments, T: performed the analysis, conducted experiments.

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Correspondence to Ratna Dini Haryuni.

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Haryuni, R.D., Lestari, W., Juliyanto, S. et al. The influence of sugar molecule type on the stability of lyophilized human serum albumin (HSA) nanocolloid kit. J Radioanal Nucl Chem 333, 1315–1322 (2024). https://doi.org/10.1007/s10967-024-09384-y

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