Physical stability of a microcrystalline beta-sitosterol suspension in oil

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Physical stability of a microcrystalline beta-sitosterol suspension in oil. / von Bonsdorff-Nikander, Anna; Karjalainen, Milja; Rantanen, Jukka; Christiansen, Leena; Yliruusi, Jouko.

In: European Journal of Pharmaceutical Sciences, Vol. 19, No. 4, 07.2003, p. 173-9.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

von Bonsdorff-Nikander, A, Karjalainen, M, Rantanen, J, Christiansen, L & Yliruusi, J 2003, 'Physical stability of a microcrystalline beta-sitosterol suspension in oil', European Journal of Pharmaceutical Sciences, vol. 19, no. 4, pp. 173-9.

APA

von Bonsdorff-Nikander, A., Karjalainen, M., Rantanen, J., Christiansen, L., & Yliruusi, J. (2003). Physical stability of a microcrystalline beta-sitosterol suspension in oil. European Journal of Pharmaceutical Sciences, 19(4), 173-9.

Vancouver

von Bonsdorff-Nikander A, Karjalainen M, Rantanen J, Christiansen L, Yliruusi J. Physical stability of a microcrystalline beta-sitosterol suspension in oil. European Journal of Pharmaceutical Sciences. 2003 Jul;19(4):173-9.

Author

von Bonsdorff-Nikander, Anna ; Karjalainen, Milja ; Rantanen, Jukka ; Christiansen, Leena ; Yliruusi, Jouko. / Physical stability of a microcrystalline beta-sitosterol suspension in oil. In: European Journal of Pharmaceutical Sciences. 2003 ; Vol. 19, No. 4. pp. 173-9.

Bibtex

@article{a82d48ca222f4e3fb6490db24459922f,
title = "Physical stability of a microcrystalline beta-sitosterol suspension in oil",
abstract = "Sterols have been shown to reduce plasma cholesterol by blocking the absorption of cholesterol from the gut. The physical properties of crystalline plant sterols limit their use in foods. A coarse-grained structure can be avoided by recrystallisation, a method that affords a reduction in the particle size. A previous work described how to produce a microcrystalline beta-sitosterol suspension. The present study deals with the stability of that suspension. Recrystallisation was carried out by two different methods; one based on rapid the other based on slow cooling, whereby six different compositions were made containing 5-30% of beta-sitosterol and secondly either 5 or 20% water was added. The particle size and habit were evaluated during a 16 weeks storage period (+4 or -19 degrees C) by way of optical microscopy. The crystal structure and degree of crystallinity was analysed by X-ray diffraction. Suspensions can, in most cases, be stored for 16 weeks without any changes to the size and habit. The only evidence of crystal growth came from a suspension with a low sterol concentration at a temperature of +4 degrees C. This is due to the dissolution-diffusion process which is affected by temperature and viscosity. Suspensions containing higher amounts of sterol remained stable, if stored at +4 or -19 degrees C, for 16 weeks. The suspensions included both hemihydrous and monohydrous beta-sitosterol crystals. Suspensions containing less sterol showed greater amounts of monohydrated crystals. This illustrates more water penetration into the crystals. A higher sterol concentration led to a larger number of smaller crystals creating reflections similar to hemihydrated crystals.",
keywords = "Cholesterol, Drug Stability, Hypolipidemic Agents, Phytosterols, Sitosterols, Soil, Suspensions, Time Factors, Viscosity, Water, X-Ray Diffraction",
author = "{von Bonsdorff-Nikander}, Anna and Milja Karjalainen and Jukka Rantanen and Leena Christiansen and Jouko Yliruusi",
year = "2003",
month = jul,
language = "English",
volume = "19",
pages = "173--9",
journal = "Norvegica Pharmaceutica Acta",
issn = "0928-0987",
publisher = "Elsevier",
number = "4",

}

RIS

TY - JOUR

T1 - Physical stability of a microcrystalline beta-sitosterol suspension in oil

AU - von Bonsdorff-Nikander, Anna

AU - Karjalainen, Milja

AU - Rantanen, Jukka

AU - Christiansen, Leena

AU - Yliruusi, Jouko

PY - 2003/7

Y1 - 2003/7

N2 - Sterols have been shown to reduce plasma cholesterol by blocking the absorption of cholesterol from the gut. The physical properties of crystalline plant sterols limit their use in foods. A coarse-grained structure can be avoided by recrystallisation, a method that affords a reduction in the particle size. A previous work described how to produce a microcrystalline beta-sitosterol suspension. The present study deals with the stability of that suspension. Recrystallisation was carried out by two different methods; one based on rapid the other based on slow cooling, whereby six different compositions were made containing 5-30% of beta-sitosterol and secondly either 5 or 20% water was added. The particle size and habit were evaluated during a 16 weeks storage period (+4 or -19 degrees C) by way of optical microscopy. The crystal structure and degree of crystallinity was analysed by X-ray diffraction. Suspensions can, in most cases, be stored for 16 weeks without any changes to the size and habit. The only evidence of crystal growth came from a suspension with a low sterol concentration at a temperature of +4 degrees C. This is due to the dissolution-diffusion process which is affected by temperature and viscosity. Suspensions containing higher amounts of sterol remained stable, if stored at +4 or -19 degrees C, for 16 weeks. The suspensions included both hemihydrous and monohydrous beta-sitosterol crystals. Suspensions containing less sterol showed greater amounts of monohydrated crystals. This illustrates more water penetration into the crystals. A higher sterol concentration led to a larger number of smaller crystals creating reflections similar to hemihydrated crystals.

AB - Sterols have been shown to reduce plasma cholesterol by blocking the absorption of cholesterol from the gut. The physical properties of crystalline plant sterols limit their use in foods. A coarse-grained structure can be avoided by recrystallisation, a method that affords a reduction in the particle size. A previous work described how to produce a microcrystalline beta-sitosterol suspension. The present study deals with the stability of that suspension. Recrystallisation was carried out by two different methods; one based on rapid the other based on slow cooling, whereby six different compositions were made containing 5-30% of beta-sitosterol and secondly either 5 or 20% water was added. The particle size and habit were evaluated during a 16 weeks storage period (+4 or -19 degrees C) by way of optical microscopy. The crystal structure and degree of crystallinity was analysed by X-ray diffraction. Suspensions can, in most cases, be stored for 16 weeks without any changes to the size and habit. The only evidence of crystal growth came from a suspension with a low sterol concentration at a temperature of +4 degrees C. This is due to the dissolution-diffusion process which is affected by temperature and viscosity. Suspensions containing higher amounts of sterol remained stable, if stored at +4 or -19 degrees C, for 16 weeks. The suspensions included both hemihydrous and monohydrous beta-sitosterol crystals. Suspensions containing less sterol showed greater amounts of monohydrated crystals. This illustrates more water penetration into the crystals. A higher sterol concentration led to a larger number of smaller crystals creating reflections similar to hemihydrated crystals.

KW - Cholesterol

KW - Drug Stability

KW - Hypolipidemic Agents

KW - Phytosterols

KW - Sitosterols

KW - Soil

KW - Suspensions

KW - Time Factors

KW - Viscosity

KW - Water

KW - X-Ray Diffraction

M3 - Journal article

C2 - 12885381

VL - 19

SP - 173

EP - 179

JO - Norvegica Pharmaceutica Acta

JF - Norvegica Pharmaceutica Acta

SN - 0928-0987

IS - 4

ER -

ID: 140622969