The Platform
More than 65% of active pharmaceutical ingredients (APIs) suffer from poor aqueous solubility. The usual fix is loading the formulation with excipients, which can cause adverse reactions and limits delivery to solid, oral pills. RapiDrugs removes the excipients entirely and conjugates the API directly with a biocompatible Bio-organic Moiety (BOM), producing a reformulated API (rAPI) that is soluble, liquid, and open to new delivery modes.
Why it works
Conjugating the API with a BOM makes the resulting molecule far more polar, so it binds water more readily. That single change is what unlocks the solubility gains across every drug we've tested. And because excipients are removed rather than added, the resulting rAPI is simpler to manufacture than a traditional formulation.
Enhanced solubility
Across our pilot NSAID molecules, rAPIs show a 100 to 1,000 fold increase in aqueous solubility compared to the parent API. For diclofenac, the two candidate BOM conjugates lifted solubility 600× and 325× over the unmodified drug.
Faster dissolution
Where the parent API can take close to two hours to fully dissolve, our rAPIs get there in around 20 minutes, a direct route to a quicker onset of action. That also opens the door to delivery formats a poorly soluble drug can't support today, like oral solutions and fast-acting injectables.
Improved in-vivo performance
In-vivo studies show our rAPIs reach the bloodstream faster and at higher concentrations than the parent drug, consistent with a faster, more predictable effect in the body. That's the kind of result that matters most to a licensing partner, since it's measured the same way regulators already evaluate a drug.
Expanding The Platform
Pilot work on a class of NSAIDs (aspirin, paracetamol, diclofenac, and ibuprofen) proved out the platform: solubility enhanced, PK improved. RapiDrugs is now applying the same rAPI approach to high-impact drugs across therapeutic areas.
Flagship Case Study
Marketed propofol is a lipid emulsion made from 10% soybean oil, 2.25% glycerol, and 1.2% egg lecithin, plus EDTA, metabisulfite, and benzyl alcohol. That formulation causes pain on injection, is susceptible to bacterial growth, and can trigger allergic reactions in patients with an egg allergy.
Lipid-free, water-clear
rAPI Propofol is a lipid-free composition with improved solubility of roughly 15 mg/mL, about 110× that of unmodified propofol. It shows no allergic reaction and no bacterial contamination risk, addressing the core failure modes of the marketed emulsion.
Safety, confirmed
Preclinical testing shows the rAPI formulation performs safely alongside the parent drug and the marketed emulsion, while reaching the bloodstream faster. Because the lipid emulsion is removed entirely, it also avoids the bacterial growth risk and egg-allergy concerns tied to the marketed version.
About Us
RapiDrugs is a deep-tech pharmaceutical startup incubated at IIT Madras Research Park, Chennai, and supported by BIRAC and ICMR. We're on a mission to make hard-to-dissolve drugs work the way they were always meant to: faster, safer, and in forms patients can actually use. Our rAPI platform started with a class of everyday NSAIDs and has since grown to include an anesthetic, an antibiotic, and several other therapeutic areas. We work closely with pharma partners to take these reformulations from lab-proven science to real, licensed products.
Incubated at IIT Madras Research Park, Chennai
Team
RapiDrugs is a deep-tech pharmaceutical startup incubated at IIT Madras Research Park, Chennai, and supported by BIRAC and ICMR.
Dr. Sanjib Senapati
Founder / Director
Shankha Banerjee
Co-founder / Director
Careers
Building a platform like ours takes more than one kind of expertise. We're growing across research, engineering, business development, and operations, so whatever you do, if you'd like to help take rAPI technology from lab to license, tell us about yourself below.
Contact
rapidrugs2024@gmail.com
IIT Madras Research Park, Chennai, India
IIT Madras Research Park · Supported by BIRAC & ICMR