Solnul® (Resistant Potato Starch)

Solanum tuberosum
Evidence Level
Limited
2 Clinical Trials
5 Documented Benefits
2/5 Evidence Score

Solnul® is an unmodified resistant potato starch, a type 2 resistant starch, made by MSP Starch Products Inc. of Carberry, Manitoba, Canada. Its trials describe a resistant starch content of 60 percent, so a 3.5 g serving supplies about 2.1 g of resistant starch. Two randomized trials of the maker's potato starch have been published, both funded at least in part by the maker and both compared with digestible corn starch. In 72 healthy adults, 3.5 g a day for 4 weeks raised stool Bifidobacterium more than placebo, while 7 g did not reach significance; hard and watery stools were counted less often on 3.5 g, a secondary result, and average gut symptom scores did not change. In an earlier 12-week trial of 30 g a day, fasting glucose and insulin fell slightly in adults over 70 but not in mid-age adults. Gas and bloating were the most common complaints.

Studied Dose 3.5 g or 7 g a day, stirred into about 125 mL of water each morning, for 4 weeks (Solnul trial); 30 g a day for 12 weeks after a 2-week placebo run-in (earlier MSPrebiotic® trial). Gas and bloating reports rose at the higher dose, so start low.
Active Compound Unmodified resistant potato starch (Solanum tuberosum), classed as type 2 resistant starch: raw starch granules that resist digestion in the small intestine and are fermented by bacteria in the colon. The trials describe a resistant starch content of 60 percent (AOAC 2002.02), so 7 g supplies about 4.2 g and 3.5 g about 2.1 g of resistant starch. The maker's earlier potato starch, MSPrebiotic®, was described as granules 15 to 100 µm across, about 80 percent amylopectin and 20 percent amylose, with 70 percent digestion resistant starch, so its 30 g dose supplied about 21 g. No published source states that MSPrebiotic® and Solnul® are the same material.

Benefits

Bifidobacterium and Akkermansia in the gut

In 72 healthy adults, 3.5 g a day for 4 weeks raised the share of Bifidobacterium in stool, the trial's main outcome, and of Akkermansia more than digestible corn starch, after outliers were removed. At 7 g a day neither rise reached significance. The trial was small, lasted 4 weeks and was funded by the maker.

Bifidobacteria and butyrate at 30 g a day

In a 12-week trial of the maker's earlier resistant potato starch at 30 g a day, Bifidobacterium rose more than on corn starch in 42 adults over 70 and in 42 adults aged 30 to 50, and stool butyrate rose slightly in the older group. These are microbiome markers; bowel movement counts did not change.

Stool form in healthy adults

In the 4-week trial, hard or lumpy stools and watery stools were less frequent on 3.5 g than on placebo among each person's last seven bowel movements, a secondary result counted per bowel movement rather than per person. Mushy or watery stools combined did not differ, 7 g did not reduce hard stools, and gut symptom scores did not change.

Fasting blood sugar and insulin in older adults

In adults over 70 without diagnosed diabetes, 30 g a day for 12 weeks lowered fasting glucose (median 5.8 to 5.5 mmol/L), fasting insulin and HOMA-IR compared with corn starch, while a second insulin resistance score did not change. Adults aged 30 to 50 showed no change. These are fasting markers, not a glucose tolerance test.

Blood fats, vitamins and choline in follow-up analyses

Post hoc analyses of the 4-week trial, led by a maker employee, reported lower serum free fatty acids, some bile acids and histamine, and higher retinol, vitamin E (alpha-tocopherol) and choline on 3.5 g a day, with no change in TMAO. In the 30 g trial, LDL cholesterol did not change overall compared with placebo.

Mechanism of action

1

Fermentation in the colon

The raw starch granules are not broken down by digestive enzymes in the small intestine, so they reach the colon, where bacteria such as Bifidobacterium ferment them into short-chain fatty acids including butyrate. Stool butyrate rose slightly in older adults on 30 g a day; the 4-week trial registered stool short-chain fatty acids as an outcome, but its published papers do not report them.

2

Responses depend on a person's gut bacteria

In the 4-week trial, Bifidobacterium and Akkermansia changes varied widely and several outliers were removed before analysis. In a study of another raw potato starch, 6 of 20 adults had no butyrate rise and no increase in the bacteria that break down resistant starch, so some people may respond little.

3

Proposed metabolic routes not yet tested

The trial authors suggested that fermentation products or gut hormones could explain the lower fasting glucose in older adults and the lower free fatty acids at 3.5 g a day. Neither trial measured gut hormones, and the fatty acid and vitamin findings come from post hoc analyses, so these routes remain unconfirmed in people.

Clinical trials

1
Solnul 3.5 g or 7 g a Day and Gut Bacteria: 4-Week Maker-Funded RCT
PubMed

Randomized, double-blind, placebo-controlled three-arm parallel trial; 7 g Solnul, 3.5 g Solnul plus 3.5 g digestible corn starch, or 7 g digestible corn starch (Amioca) each morning for 4 weeks; registered NCT05242913 about two years after the trial ended; funded by MSP Starch Products, which employs the first author, with the trial run under contract by Nutrasource and two authors former maker consultants; five follow-up papers (2023 to 2025), one not indexed in PubMed, come from this trial (Bush et al. 2023, Nutrients)

75 healthy adults aged 18 to 69 with a BMI of 18 to 34.9 were randomized, 25 per arm, and 72 were analyzed (average age about 38, 69 percent women). People with IBS or other digestive disorders were excluded.

Primary outcome: Bifidobacterium rose more on 3.5 g than on placebo (p = 0.038) after outliers were removed, but not on 7 g (p = 0.14). Akkermansia rose more on 3.5 g (p = 0.014) but not on 7 g (p = 0.056). Among the last seven bowel movements per person, type 1 or 2 stools were fewer on 3.5 g (9 versus 23 of 168, p = 0.0085) and type 7 stools fewer (0 versus 6, p = 0.03), while type 6 or 7 stools did not differ (19 versus 13); on 7 g only types 5 to 7 differed. A secondary analysis found no change in average pain, belching, bloating, gas or wellbeing scores in any arm.

2
MSPrebiotic 30 g a Day in Older and Mid-Age Adults: 12-Week RCT
PubMed

Randomized, double-blind, placebo-controlled trial; 2-week corn starch run-in for all, then 30 g/day of MSPrebiotic® resistant potato starch (the maker's earlier potato starch, stated to be 70 percent resistant starch versus 60 percent for Solnul) or digestible corn starch (Amioca TF) for 12 weeks; registered NCT01977183; funded by the National Research Council of Canada and MSPrebiotics Inc., which supplied both products; glucose and LDL results appear in two companion papers, one written by a maker employee (Alfa et al. 2018, Clin Nutr)

84 adults who completed the study: 42 aged 70 or older (11 living in long-term care) and 42 aged 30 to 50, without diagnosed diabetes or prediabetes; about 21 per group.

Bifidobacterium rose more than on placebo in both age groups (p = 0.047 older, p = 0.006 mid-age), and stool butyrate rose slightly in older adults. In older adults, fasting glucose (p = 0.03), insulin (p = 0.009) and HOMA-IR (p = 0.009) changed more favorably than on placebo, with glucose about 7 percent lower; LP-IR did not differ, and no glucose or insulin measure changed in mid-age adults. Pain, bloating and flatulence scores stayed low and did not differ from placebo, bowel movement counts did not change, and LDL cholesterol did not change overall.

Side effects and drug interactions

Common Potential side effects

In the 4-week trial, digestive events judged possibly related to the product (gas, bloating, belching, abdominal pain) occurred in 9 of 50 people on Solnul and 2 of 25 on placebo; the paper's text places most of them in the 7 g arm and its table in the 3.5 g arm. No serious events occurred and none led to withdrawal.
At 30 g a day for 12 weeks, abdominal pain, bloating and flatulence scores stayed low (2 or less on a 5 point scale) and did not differ from corn starch.
The longest published trial lasted 12 weeks, so longer-term safety data are lacking. Increase the amount gradually if gas or bloating occurs.

Important Drug interactions

Diabetes medicines: in adults over 70, 30 g a day slightly lowered fasting glucose and insulin. If you take glucose-lowering medicine, check your blood sugar when you start and talk to your prescriber.
Other oral medicines: in the 30 g trial, participants took the starch at least 2 hours before or after other medicines. No drug interaction studies have been published; ask your pharmacist about spacing doses.

Frequently asked questions about Solnul® (Resistant Potato Starch)

What is Solnul?

Solnul is an unmodified resistant potato starch made by MSP Starch Products in Manitoba, Canada. It is a type 2 resistant starch with a stated resistant starch content of 60 percent. It passes undigested to the colon, where gut bacteria ferment it.

How much Solnul was used in studies?

The Solnul trial used 3.5 g or 7 g a day stirred into water for 4 weeks; only the 3.5 g dose raised Bifidobacterium significantly. The maker's earlier potato starch was tested at 30 g a day for 12 weeks. Follow the product label and start with a small amount.

Does Solnul cause gas or bloating?

It can. In the 4-week trial, possibly related gas, bloating, belching or abdominal pain occurred in 9 of 50 people on the starch and 2 of 25 on placebo, with no serious events. At 30 g a day for 12 weeks, symptom scores stayed low and did not differ from placebo.

How is Solnul different from other resistant starch supplements?

Most resistant starch research used high-amylose maize starch or raw potato starch at 30 to 45 g a day. Solnul was studied at much lower doses of 3.5 to 7 g a day, mainly for gut bacteria changes. Results from one starch or dose cannot be assumed for another.

What is Solnul used for?

NutraSmarts does not list Solnul under a health category. What the research covers: In 72 healthy adults, 3.5 g a day for 4 weeks raised the share of Bifidobacterium in stool, the trial's main outcome, and of Akkermansia more than digestible corn starch, after outliers were removed.

Is Solnul safe, and does it have side effects?

Side effects and cautions reported for Solnul include: In the 4-week trial, digestive events judged possibly related to the product (gas, bloating, belching, abdominal pain) occurred in 9 of 50 people on Solnul and 2 of 25 on placebo; the paper's text places most of them in the 7 g arm and its table in the 3.5 g arm. It may also interact with some medications. Solnul is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Solnul interact with any medications?

Possible interactions include: Diabetes medicines: in adults over 70, 30 g a day slightly lowered fasting glucose and insulin. If you take glucose-lowering medicine, check your blood sugar when you start and talk to your prescriber. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Solnul?

NutraSmarts rates the evidence for Solnul as Limited (2 out of 5). It is backed by 2 study summaries and 12 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(12 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Bush JR, Baisley J, Harding SV, Alfa MJ. Consumption of Solnul(™) Resistant Potato Starch Produces a Prebiotic Effect in a Randomized, Placebo-Controlled Clinical Trial. Nutrients. 2023;15(7):1582. doi: 10.3390/nu15071582.PubMedUsed to support: Randomized, double-blind, placebo-controlled three-arm trial of Solnul (named in the methods; unmodified type 2 resistant potato starch with 60 percent resistant starch) at 7 g or 3.5 g a day versus 7 g of digestible corn starch for 4 weeks in 75 healthy adults (72 analyzed). The registered primary outcome, the rise in stool Bifidobacterium, was greater than placebo on 3.5 g (p = 0.038, after outlier removal) but not on 7 g (p = 0.14); Akkermansia rose on 3.5 g (p = 0.014) but not on 7 g (p = 0.056). Counted per bowel movement, hard or lumpy stools and watery stools were less frequent on 3.5 g, and loose stools (types 5 to 7) on 7 g. No serious adverse events. Funded by MSP Starch Products, which employs the first author; registered NCT05242913 after the trial ended.
  2. Bush JR, Alfa MJ. Consumption of resistant potato starch produces changes in gut microbiota that correlate with improvements in abnormal bowel symptoms: a secondary analysis of a clinical trial. BMC Nutr. 2024;10(1):152. doi: 10.1186/s40795-024-00962-7.PubMedUsed to support: Post hoc analysis of the same 4-week Solnul trial (70 healthy adults; 3.5 g or 7 g a day or placebo). Average daily scores for abdominal pain, belching, bloating, gas and feeling unwell were low at baseline and did not change in any arm. The paper reports correlations between symptom changes and changes in several bacterial groups, whose average abundance did not change with treatment. Authors are a maker employee and a maker consultant; registered NCT05242913.
  3. Bush JR, Iwuamadi I, Han J, Schibli DJ, Goodlett DR, Deehan EC. Resistant Potato Starch Supplementation Reduces Serum Free Fatty Acid Levels and Influences Bile Acid Metabolism. Metabolites. 2024;14(10):536. doi: 10.3390/metabo14100536.PubMedUsed to support: Exploratory post hoc analysis of stored serum from the 4-week Solnul trial (3.5 g a day versus placebo): total serum free fatty acids and some taurine- and glycine-conjugated secondary bile acids fell relative to placebo, and ketone bodies did not change. First author employed by MSP Starch Products, which contracted the metabolomic testing and paid the publication charge.
  4. Bush JR, Han J, Goodlett DR. Resistant Potato Starch Supplementation Increases Serum Antioxidant Levels in a Randomized Trial. Metabolites. 2025;15(10):661. doi: 10.3390/metabo15100661.PubMedUsed to support: Post hoc serum metabolomic analysis of the 4-week Solnul trial (3.5 g a day, n = 24, versus placebo, n = 24; NCT05242913): serum all-trans retinol and alpha-tocopherol rose on the starch, coenzyme Q10 rose in both groups, and uric acid, hippuric acid and two markers of advanced glycation did not change. First author employed by MSP Starch Products, which contracted the testing and paid the publication charge.
  5. Bush JR, Han J, Goodlett DR. Resistant Potato Starch Supplementation Increases the Serum Levels of Choline and Sphingomyelins Without Affecting Trimethylamine Oxide Levels. Metabolites. 2025;15(10):662. doi: 10.3390/metabo15100662.PubMedUsed to support: Post hoc serum analysis of the 4-week Solnul trial (3.5 g a day versus placebo): serum choline and several sphingomyelins rose and trimethylamine fell on the starch, while trimethylamine oxide (TMAO) did not change. First author employed by MSP Starch Products, which contracted the testing and paid the publication charge.
  6. Alfa MJ, Strang D, Tappia PS, Graham M, Van Domselaar G, Forbes JD, Laminman V, Olson N, DeGagne P, Bray D, Murray BL, Dufault B, Lix LM. A randomized trial to determine the impact of a digestion resistant starch composition on the gut microbiome in older and mid-age adults. Clin Nutr. 2018;37(3):797-807. doi: 10.1016/j.clnu.2017.03.025. Epub 2017 Mar 31..PubMedUsed to support: Randomized, double-blind, placebo-controlled trial of MSPrebiotic, the maker's resistant potato starch, at 30 g a day for 12 weeks versus corn starch, in 42 adults aged 70 or older and 42 aged 30 to 50 who completed the study. Bifidobacterium rose more than on placebo in both age groups (p = 0.047 and p = 0.006), stool butyrate rose slightly in the older group, and the higher baseline Proteobacteria seen in older adults was no longer seen after 12 weeks on the starch. Registered NCT01977183.
  7. Alfa MJ, Strang D, Tappia PS, Olson N, DeGagne P, Bray D, Murray BL, Hiebert B. A Randomized Placebo Controlled Clinical Trial to Determine the Impact of Digestion Resistant Starch MSPrebiotic(®) on Glucose, Insulin, and Insulin Resistance in Elderly and Mid-Age Adults. Front Med (Lausanne). 2017;4:260. doi: 10.3389/fmed.2017.00260. eCollection 2017..PubMedUsed to support: Companion paper from the same 12-week MSPrebiotic trial (30 g a day versus corn starch, after a 2-week placebo run-in). In adults over 70 without diagnosed diabetes or prediabetes, fasting glucose (p = 0.03), insulin (p = 0.009) and HOMA-IR (p = 0.009) changed more favorably than on placebo; LP-IR did not differ, and adults aged 30 to 50 showed no change. Gut symptom scores stayed low and did not differ from placebo. Funded by the National Research Council of Canada and MSPrebiotics Inc., which supplied the products.
  8. Bush JR, Alfa MJ. Increasing levels of Parasutterella in the gut microbiome correlate with improving low-density lipoprotein levels in healthy adults consuming resistant potato starch during a randomised trial. BMC Nutr. 2020;6(1):72. doi: 10.1186/s40795-020-00398-9.PubMedUsed to support: Exploratory analysis of 75 participants from the 12-week MSPrebiotic trial (38 on the starch, 37 on placebo): Parasutterella tended to rise on the starch (p = 0.07), and its rise correlated with falling LDL cholesterol in the starch group only; LDL did not change overall compared with placebo. Funded by MSP Starch Products, which employs the first author.
  9. Shamloo M, Mollard R, Wang H, Kingra K, Tangri N, MacKay D. A randomized double-blind cross-over trial to study the effects of resistant starch prebiotic in chronic kidney disease (ReSPECKD). Trials. 2022;23(1):72. doi: 10.1186/s13063-022-06009-1.PubMedUsed to support: Published protocol, not results: a randomized double-blind crossover trial (NCT04961164) giving MSPrebiotic resistant potato starch, 15 g twice a day, or corn starch to adults with chronic kidney disease, with blood uremic toxins as the primary outcome. ClinicalTrials.gov lists the trial as completed in November 2024; no results paper was found in PubMed or Europe PMC.
  10. Venkataraman A, Sieber JR, Schmidt AW, Waldron C, Theis KR, Schmidt TM. Variable responses of human microbiomes to dietary supplementation with resistant starch. Microbiome. 2016;4(1):33. doi: 10.1186/s40168-016-0178-x.PubMedUsed to support: Other product (unmodified raw potato starch, brand not named in the abstract), not Solnul. In 20 healthy young adults, average stool butyrate rose from 8 to 12 mmol/kg, but 6 people had no rise and no increase in the bacteria that break down resistant starch (Bifidobacterium adolescentis or Ruminococcus bromii).
  11. Snelson M, Jong J, Manolas D, Kok S, Louise A, Stern R, Kellow NJ. Metabolic Effects of Resistant Starch Type 2: A Systematic Literature Review and Meta-Analysis of Randomized Controlled Trials. Nutrients. 2019;11(8):1833. doi: 10.3390/nu11081833.PubMedUsed to support: Other products (type 2 resistant starch of several kinds), not Solnul. Meta-analysis of 22 randomized trials (670 participants) giving at least 8 g/day: triglycerides fell slightly in healthy people and body weight fell 1.29 kg in people with type 2 diabetes, both driven by a few studies; there was no effect on other outcomes, including fasting glucose and insulin resistance. The authors concluded short-term use is of limited cardiometabolic benefit.
  12. Bush JR, Han J, Deehan EC, Harding SV, Maiya M, Baisley J, Schibli D, Goodlett DR. Resistant potato starch supplementation reduces serum histamine levels in healthy adults with links to attenuated intestinal permeability. J Funct Foods. 2023;108:105740. doi: 10.1016/j.jff.2023.105740.SourceUsed to support: Not PubMed-indexed (open-access journal article; abstract read from its DOI record). Post hoc serum metabolomic analysis of the 4-week Solnul trial, 3.5 g a day versus placebo (48 people): serum histamine fell on the starch while histamine breakdown products did not change, and some serum metabolites the authors link to gut permeability (5-hydroxylysine, acetylspermidine, carnitine ratios) fell. No direct gut permeability test is described. The first author is affiliated with MSP Starch Products; the funding statement was not read.