Effects of cellulose derivatives and poly(ethylene oxide)-poly(propylene oxide) tri-block copolymers (Pluronic® surfactants) on the properties of alginate based microspheres and their interactions with phagocytic cells

Argaw Kidane, Paul Guimond, Tzu Chi Rob Ju, Margaret Sanchez, Janet Gibson, Adam North, Harm HogenEsch, Terry L. Bowersock

Research output: Contribution to journalArticle

15 Citations (Scopus)

Abstract

The goal of this study was to examine the phagocytosis of alginate based microspheres with different surface properties. Favorable interaction with macrophages is critical for uptake subsequent processing of the microspheres used for oral vaccine delivery. We examined the effects of size of alginate microspheres and hydrophobicity on cellular uptake. We also examined the toxicity of formulation components to phagocytic cells. Alginate microspheres were made by the emulsion-cross-linking technique. Five different formulations of microspheres were evaluated for size, hydrophobicity, cellular uptake and toxicity to macrophages. The formulations examined were: alginate alone (A), alginate with methylcellulose (AA) AA with Pluronic®L61 (AA61), alginate with hydroxypropyl methylcellulose (AK3), and AK3 with Pluronic® L61 (AK3 61). Microspheres with without poly-L-lysine (PLL) coating were tested. The mean volume sizes of A, AA, AA61, AK3, AK3 61 microspheres (MS) were 11, 10.5, 3.8, 8.7 and 3.9 μm, respectively. After coating them with PLL the mean volume sizes were 10.4, 10, 3.7, 8.8 and 3.5 μm, respectively. Hydrophobicity of the microspheres was evaluated by measuring contact angle on a glass slide coated with the microspheres. The contact angles measured using a goniometer on A, AA, AA61, AK3, AK3 61 MS were 20, 34.8, 71, 29 and 80°, respectively whereas those MS coated with PLL were 49.7, 55.8, 91, 48.25 and 84.4°, respectively. Cellular uptake studies using flow cytometery revealed that AA61 MS coated with PLL were phagocytosed most often by mouse macrophages. There was no statistically significant difference in cellular uptake among those MS without PLL coating. Toxicity to macrophages was shown to depend on the ratio of microspheres to cells. These studies suggest that formulation can dramatically affect the physical characteristics of alginate MS in ways that can affect how they will interact with cells in the body when administered as a vaccine delivery system.

Original languageEnglish (US)
Pages (from-to)181-189
Number of pages9
JournalJournal of Controlled Release
Volume85
Issue number1-3
DOIs
StatePublished - Dec 13 2002

Fingerprint

Poloxamer
Ethylene Oxide
Phagocytes
Microspheres
Surface-Active Agents
Cellulose
Lysine
Macrophages
Hydrophobic and Hydrophilic Interactions
polypropylene glycol
alginic acid
Phagocytosis
Vaccines
Methylcellulose
Surface Properties
Emulsions

Keywords

  • Microspheres
  • Mucosal immunity
  • Vaccine delivery
  • Vaccines

ASJC Scopus subject areas

  • Pharmaceutical Science

Cite this

Effects of cellulose derivatives and poly(ethylene oxide)-poly(propylene oxide) tri-block copolymers (Pluronic® surfactants) on the properties of alginate based microspheres and their interactions with phagocytic cells. / Kidane, Argaw; Guimond, Paul; Ju, Tzu Chi Rob; Sanchez, Margaret; Gibson, Janet; North, Adam; HogenEsch, Harm; Bowersock, Terry L.

In: Journal of Controlled Release, Vol. 85, No. 1-3, 13.12.2002, p. 181-189.

Research output: Contribution to journalArticle

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abstract = "The goal of this study was to examine the phagocytosis of alginate based microspheres with different surface properties. Favorable interaction with macrophages is critical for uptake subsequent processing of the microspheres used for oral vaccine delivery. We examined the effects of size of alginate microspheres and hydrophobicity on cellular uptake. We also examined the toxicity of formulation components to phagocytic cells. Alginate microspheres were made by the emulsion-cross-linking technique. Five different formulations of microspheres were evaluated for size, hydrophobicity, cellular uptake and toxicity to macrophages. The formulations examined were: alginate alone (A), alginate with methylcellulose (AA) AA with Pluronic{\circledR}L61 (AA61), alginate with hydroxypropyl methylcellulose (AK3), and AK3 with Pluronic{\circledR} L61 (AK3 61). Microspheres with without poly-L-lysine (PLL) coating were tested. The mean volume sizes of A, AA, AA61, AK3, AK3 61 microspheres (MS) were 11, 10.5, 3.8, 8.7 and 3.9 μm, respectively. After coating them with PLL the mean volume sizes were 10.4, 10, 3.7, 8.8 and 3.5 μm, respectively. Hydrophobicity of the microspheres was evaluated by measuring contact angle on a glass slide coated with the microspheres. The contact angles measured using a goniometer on A, AA, AA61, AK3, AK3 61 MS were 20, 34.8, 71, 29 and 80°, respectively whereas those MS coated with PLL were 49.7, 55.8, 91, 48.25 and 84.4°, respectively. Cellular uptake studies using flow cytometery revealed that AA61 MS coated with PLL were phagocytosed most often by mouse macrophages. There was no statistically significant difference in cellular uptake among those MS without PLL coating. Toxicity to macrophages was shown to depend on the ratio of microspheres to cells. These studies suggest that formulation can dramatically affect the physical characteristics of alginate MS in ways that can affect how they will interact with cells in the body when administered as a vaccine delivery system.",
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