The delivery science

The dose on
the box,
delivered.

Every supplement is sold on what goes into it. The number that decides whether it works is how much of that ever reaches your blood. This page is the physiology of that gap, the route we take instead, and the limits of what either can tell you.

Dose still intact on arrival
Swallowed
A fraction of the label. How much depends on the compound.
Strip2Cell film
90%Up to*

*Up to 90% is the ceiling of the sublingual route for actives suited to it, drawn from published pharmacology — not a claim about a specific outcome. We publish no figure for pills or gummies, because it changes with the compound.

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01 — The problem

Your liver gets first pick.

Anything you swallow takes the long route. It has to survive the stomach, cross the wall of the small intestine, and then pass through the liver — where enzymes metabolise a share of it — before a single molecule reaches general circulation. Pharmacologists call that last step first-pass metabolism.

It is why the figure printed on a panel and the figure in your blood are two different numbers. Not a defect in the formula. A property of the route.

Goodman & Gilman · The Pharmacological Basis of Therapeutics
01Stomach

Acid, then enzymes

Breakdown starts before absorption does. Botanicals and peptides are the least forgiving of this stage.

02Small intestine

Only part crosses

What survives has to pass the gut wall. What it finds there — food, timing, your own gut — changes the answer nightly.

03Liver, then blood

The first pass

Everything absorbed from the gut is routed to the liver first, where enzymes metabolise a share of the dose. What survives that is the only part that ever had a job to do — an hour or more after you swallowed it.

02 — The shortcut

The tissue under your tongue was built for this.

The floor of your mouth is one of the most permeable surfaces on the body: a thin, non-keratinised membrane sitting directly over a dense bed of capillaries. Anything that crosses it enters the veins draining the head and neck — which feed general circulation without passing through the liver.

No stomach. No gut wall. No first pass. Delivered this way, compounds suited to the route reach far more of the bloodstream than the same compounds swallowed.

British Journal of Clinical Pharmacology, 2018
Film Mucosa Bloodstream → systemic circulation
Where it happens

A membrane, then blood

The film holds itself against the mucosa while it dissolves, so the actives are released exactly where the tissue is thinnest and the capillaries are closest.

01
Thin, non-keratinised membrane

Nothing like the barrier lining your gut. It is built to let things through.

02
A dense capillary bed beneath it

Blood sits millimetres from the surface, which is why absorption starts in minutes rather than an hour.

03
Straight into systemic circulation

The veins draining your mouth do not route through the liver, so nothing is metabolised before it can work.

Borrowed, not invented

Medicine has used this route for decades: nitroglycerin placed under the tongue for angina, sublingual B12, prescription oral films. We did not discover the shortcut. We built a nightly supplement around it.

03 — Format

Same actives.
Different arrival.

A capsule, a gummy and a film can carry an identical ingredient panel. Two of them take the route through the gut and the liver, so what arrives is decided by physiology rather than by the label. The third does not take that route at all.

Bar length = dose reaching the bloodstreamSteel = the swallowed route
Strip2Cell film
Mucosa → bloodstream
≤90%
Capsule or tablet
Gut → liver → bloodstream
A fraction
Gummy
The same route, plus sugar
A fraction
Liquid
Faster to the gut, same liver
A fraction

The two lower bars carry no percentage on purpose. Published bioavailability for swallowed compounds spans a wide range depending on the molecule, the meal and the person, so a single tidy percentage would be a design decision rather than a fact. Ours is stated as a ceiling, with an asterisk, for the same reason.

04 — The signal

A plant signal, not a synthetic dose.

Melatonin is not a sedative. It is a timing cue — the molecule that tells your body which part of the day it is. Plants make the same compound, and pistachios are among the richest natural sources of it. That plant-derived form is phytomelatonin, and it arrives with the cofactors the nut carries rather than isolated in a lab.

The heaviness people associate with sleep aids is largely a dosing artefact: a cue delivered too strongly, or too late, is still in your system at seven in the morning. Research on low, well-timed doses finds circadian phase shifts without next-day grogginess.

Cell Reports Medicine, 2023
01

It works with the rhythm

A cue, not a switch. Your body still runs the night; the strip tells it the night has started.

02

Delivered with its cofactors

100mg of pistachio extract per strip, carrying phytomelatonin in the form the plant made it.

03

Nothing to clear at breakfast

No synthetic melatonin in the formula, and no escalating dose to keep it working on night thirty.

05 — The formula, by mechanism

Three ways a night fails.

A sleepless night is rarely one problem. There is the mind that will not stop, the body that will not drop off, and the morning that arrives heavier than it should. Each active in the strip is there for one of those three.

Failure 01

Can't switch off

Lights out, mind still running the day. This is excitation that has not been braked.

10mg
GABA

The brain's principal inhibitory neurotransmitter — the brake on cortical activity, supplied directly rather than coaxed.

10mg
Passion flower

Flavonoids that act on the same GABA-A receptor, traditionally used for the nights that end wired rather than tired.

Failure 02

Can't drop off

Calm enough, but the gap between lying down and being asleep keeps stretching.

100mg
Pistachio extract · phytomelatonin

The timing cue that opens the door. Absorbed sublingually, it reaches circulation while you are still putting your phone down.

10mg
Valerian root

Valerenic acid interacts with GABA-A signalling. Pooled trials associate valerian with improved subjective sleep quality — Bent et al., The American Journal of Medicine, 2006.

Failure 03

Wake up groggy

You slept. You just did not arrive in the morning with it. Usually a dose still in the system.

10mg
Chamomile · apigenin

The flavone behind the cup, at a dose a cup cannot reach. It binds GABA-A benzodiazepine sites weakly — calming without the sedation profile of a drug.

0mg
Synthetic melatonin

Deliberately absent. The morning is part of the product, so nothing in the formula is designed to outlast the night.

Per strip
Dose
Mechanism
Pistachio extract
100mg
Phytomelatonin — circadian timing cue
GABA
10mg
Inhibitory neurotransmitter — reduces excitation
Valerian root
10mg
Valerenic acid — GABA-A signalling, sleep onset
Passion flower
10mg
Flavonoids — GABA-A modulation
Chamomile
10mg
Apigenin — weak benzodiazepine-site binding

Doses are per strip, as printed on the box. Other ingredients: Pullulan, Monk Fruit Extract, Cellulose, Lecithin, Mixed Berry Flavour, Sorbitol Syrup, Steviol Glycosides. Zero sugar.

06 — Manufacturing & testing

Held to the dose on the box.

A delivery claim is only worth what the manufacturing behind it is worth. Every batch is made in a certified facility, cast and cut so each strip carries the same dose, and tested by a third party against the printed panel before it ships.

01

GMP, HACCP, ISO 22000

Manufactured to pharmaceutical process standards, not food-supplement minimums.

02

Third-party tested, every batch

Potency and purity, batch by batch — not once at launch and quoted forever.

03

Dose uniformity by design

The film is cast to a fixed thickness and cut to a fixed area, so strip thirty matches strip one.

04

Single-dose sachets

Each strip is sealed on its own. No open bottle slowly oxidising on a bedside table.

05

No proprietary blends

Every active is listed at its milligram figure. A blend name is a way to hide a small dose.

06

Certificate of analysis on request

Quote the batch number printed on your box and we send the report for that batch.

GMP certifiedHACCPISO 22000:2018Zero sugarEngineered in Singapore
07 — Limits

What we don't claim.

A science page that only argues one way is marketing. Here is the other half — the things the evidence does not let us say, stated plainly so you can weigh the rest.

01

It is not a sedative

The strip supports the body's own wind-down. It does not switch you off, and it is not a treatment for insomnia or any medical condition.

02

Up to 90% is a ceiling

It describes what the sublingual route can reach for compounds suited to it, from published pharmacology. It is not a measurement of one person on one night.

03

The route is studied; this formula is not a trial

The evidence we cite is on delivery and on individual actives. We have not run a clinical trial on the finished strip, and we will not imply that we have.

04

Nights differ, people differ

Caffeine, stress, screens and shift work all outweigh a supplement. The strip is the easy part of a night, not the whole of it.

Dr.Strips+ Sleep is a health supplement, not a medicine, and is not intended to diagnose, treat, cure or prevent any disease. Statements on this page have not been evaluated by the HSA. If you are pregnant, breastfeeding, on medication or under medical care, speak to your doctor first.

08 — The receipts

Where the science comes from.

Each claim above, and the published work it rests on. Bioavailability figures are compound-dependent ranges from the literature, not outcomes measured on this product.

First-pass metabolism reduces the dose reaching circulation
Goodman & Gilman · The Pharmacological Basis of Therapeutics
Sublingual delivery reaches up to 90% bioavailability for suited compounds
British Journal of Clinical Pharmacology, 2018
Low, well-timed melatonin cues circadian phase without next-day grogginess
Cell Reports Medicine, 2023
Valerian is associated with improved subjective sleep quality across pooled trials
Bent et al. · The American Journal of Medicine, 2006
Apigenin binds benzodiazepine sites on the GABA-A receptor with low affinity
Viola et al. · Planta Medica, 1995
Pistachios are among the richest dietary sources of plant melatonin
Published phytomelatonin content analyses
09 — Our standard

The science behind better supplementation.

Science isn't a badge. It's a process.

At Dr.Strips+, we use evidence to guide how we think about ingredients, formulations and product claims.

We look beyond headlines. We look at:

01
Study design
02
Dosage
03
Population
04
Outcomes
05
Consistency
06
Limitations
07
Whether it applies to this product

Because a scientific ingredient doesn't automatically make a scientific product. The details matter.

The whole point

Read it once.
Then just sleep.

Thirty strips, thirty nights. Ten minutes before bed, one on your tongue, and none of this to think about again.

30-night guarantee