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Characterisation of chewed/sucked and expectorated raw almonds

The role of plant cell walls in regulating starch and lipid bioaccessibility from plant foods: in silico, in vivo and in vitro studies

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN58438021
Enrollment
15
Registered
2013-11-13
Start date
2011-04-15
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Digestion and nutrient bioaccessibility Nutritional, Metabolic, Endocrine

Interventions

Volunteers are randomly allocated to treatments using an electronic randomisation program 1. Mastication and expectoration of whole raw and roasted almonds. 2. Mastication and expectoration of muffin

Sponsors

King's College London (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Be generally healthy 2. Healthy dentition 3. Be at least 18 years old 4. Have eaten almonds with no adverse effects

Exclusion criteria

Exclusion criteria: You must not: 1. Be allergic to nuts of any kind 2. Be allergic to celery, pears, apples, cherries, peaches or parsley 3. Have any teeth missing (apart from unerupted wisdom teeth) 4. Have bleeding gums 5. Had dental treatment (other than checkups) in the last 3 months 6. Be currently suffering from any infectious disease that may be passed on via saliva e.g. Glandular fever, flu 7. Be allergic to wheat, gluten or milk, if chewing the almond muffin meals

Design outcomes

Primary

MeasureTime frame
Measure the size of almond particles that have been chewed sufficiently to be swallowed. Mechanical sieving and laser diffraction are used to measure particle size distribution of the expectorated and digested almonds.

Secondary

MeasureTime frame
1. Find shape parameters (numerical values) that describe the general particle shape to allow the theoretical model to predict lipid release from intact cells: examined by microscopy (light, scanning electron and transmission) 2. Measure any changes in lipid content and cell-wall polysaccharide composition due to chewing. Quantifying the amount of lipid lost using the Soxhlet method and cell wall changes by gas chromatography. 3. Determine whether cooking almonds affects the release of lipid from the chewed almonds: examined by microscopy (light, scanning electron and transmission) 4. Determine whether lipid is removed from ruptured cells only when in the presence of saliva: examined by microscopy (light, scanning electron and transmission) 5. Determine the effects of chewing on lipid release and cell-wall structure during simulated gastric (stomach) digestion. Quantifying the amount of lipid lost using the Soxhlet method and cell wall changes by gas chromatography. 6. Evaluate how almond incorporated into a complex food structure (muffin) behaves following chewing and simulated digestion. Quantifying the amount of lipid lost using the Soxhlet method and cell wall changes by gas chromatography. Time points: 1. Baseline (analysis of raw and roasted almonds, and muffins) 2. After mastication 3. During/after gastric digestion (various time points depending on the test food, i.e. almond vs muffin) 4. After duodenal digestion Chewed almond and muffins are loaded into an in vitro digestion model (Dynamic Gastric Model at the Institute of Food Research in Norwich)

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026