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In-use stability of Rituximab and IVIG during intravenous infusion: Impact of peristaltic pump, IV bags, flow rate, and plastic syringes.
Hada, Shavron; Shin, I Jeong; Park, Ha Eun; Kim, Ki Hyun; Kim, Kwang Joon; Jeong, Seong Hoon; Kim, Nam Ah.
Affiliation
  • Hada S; BK21 FOUR Team and Integrated Research Institute for Drug Development, College of Pharmacy, Dongguk University, Gyeonggi 10326, Republic of Korea. Electronic address: shavron.hada@dgu.ac.kr.
  • Shin IJ; BK21 FOUR Team and Integrated Research Institute for Drug Development, College of Pharmacy, Dongguk University, Gyeonggi 10326, Republic of Korea.
  • Park HE; BK21 FOUR Team and Integrated Research Institute for Drug Development, College of Pharmacy, Dongguk University, Gyeonggi 10326, Republic of Korea.
  • Kim KH; Department of Pharmacy, College of Pharmacy, Mokpo National University, Muan 58554, Republic of Korea.
  • Kim KJ; College of Pharmacy, Chonnam National University, Gwangju 61186, Republic of Korea.
  • Jeong SH; BK21 FOUR Team and Integrated Research Institute for Drug Development, College of Pharmacy, Dongguk University, Gyeonggi 10326, Republic of Korea. Electronic address: shjeong@dongguk.edu.
  • Kim NA; Department of Pharmacy, College of Pharmacy, Mokpo National University, Muan 58554, Republic of Korea; Department of Biomedicine, Health & Life Convergence Sciences, BK21 Four, Biomedical and Healthcare Research Institute, Mokpo National University, Muan 58554, Republic of Korea. Electronic addr
Int J Pharm ; 663: 124577, 2024 Sep 30.
Article in En | MEDLINE | ID: mdl-39137820
ABSTRACT
This study investigates the impact of intravenous (IV) infusion protocols on the stability of Intravenous Immunoglobulin G (IVIG) and Rituximab, with a particular focus on subvisible particle generation. Infusion set based on peristaltic movement (Medifusion DI-2000 pump) was compared to a gravity-based infusion system (Accu-Drip) at different flow rates. The impacts of different diluents (0.9 % saline and 5.0 % dextrose) and plastic syringes with or without silicone oil (SO) were also investigated. The results from the aforementioned particular case demonstrated that peristaltic pumps generated high levels of subvisible particles (prominently < 25 µm), exacerbated by increasing flow rates, specifically in formulations lacking surfactants. Other factors, such as diluent type and syringe composition, also increased the number of subvisible particles. Strategies that can help overcome these complications include surfactant addition as well as the use of SO-free syringes and a gravity infusion system, which aid in reducing particle formation and preserving antibody monomer during administration. Altogether, these findings highlight the importance of the careful selection of formulations and infusion protocols to minimize particle generation during IV infusion both for patients' safety and treatment efficacy.
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Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Syringes / Immunoglobulins, Intravenous / Drug Stability / Rituximab Limits: Humans Language: En Journal: Int J Pharm Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Syringes / Immunoglobulins, Intravenous / Drug Stability / Rituximab Limits: Humans Language: En Journal: Int J Pharm Year: 2024 Document type: Article Country of publication: