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8 min read
10/31/25

Liquid-to-Solid Dose Conversion for Safety and Compliance

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Formulating for rare and pediatric diseases presents unique obstacles: small patient populations, strict excipient limits, and the need for accurate, palatable dosing, every decision carries weight.

Liquid medications, while familiar, often susceptible to microbial growth, inconsistent dosing, and temperature-sensitive storage. Converting these liquids and suspensions into mini tablets or ODTs offers a safer, more stable, and patient-friendly alternative.

The Orphan Drug Challenge


These therapies demand smarter formulation choices that can make development viable, stable, and safe at any scale. The need is significant.

Rare diseases affect an estimated 300 million people worldwide (1 in 20), yet fewer than 10% of known conditions have an approved treatment.


Despite growing demand, orphan drug programs face limited patient reach and high development costs that make formulation efficiency essential. Every excipient, every stability parameter, and every patient experience matters, especially for pediatric therapies where compliance and safety define success.

Behind every rare or pediatric formulation is a patient population too small to attract large-scale investment, yet too critical to overlook.

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Why Orphan Drug Development Demands More Precision

With small-scale populations and narrow safety margins, success depends on stable, patient-friendly formulations that can reach those who need them most.

⚠️ Over 300 children died from contaminated cough syrups in 2022-2025 — Solid dosage forms reduce this risk.


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UltraBurst™ Platform Technology

Built for formulators ready to move beyond liquid limits. Suitable for:

• Pediatric syrups
• Antihistamine or antibiotic suspensions
• Pain management
• Nutritional supplements
• Orphan drug formulations targeting rare metabolic, genetic, and oncology conditions.

Designed for 503A and 503B facilities, specialty compounders, and pediatric-focused pharmacies.

Sample UltraBursttablety-2155684970


Performance Highlights:

✔️ High-Dose APIs: Handles challenging active ingredients with excellent compactibility
✔️ Rapid Dissolution: Tablets dissolve in seconds for immediate relief
✔️ Pediatric-Optimized: Easy to consume, patient-friendly formulations
✔️ Content Uniformity: Precise dosing for small patient populations

Check out UltraBurst technology

Case Study: Diphenhydramine Mini ODTs

•  API:  Taste-Masked APAP (Acetaminophen)
•  Challenge: High dose API with compactibility and content uniformity issues
•  Solution:  Liquid suspension successfully converted to mini ODT using UltraBurst™ technology


Results:


✅ Quick dissolving tablet (12 seconds)
✅ Easy to consume and patient-friendly
✅ Accurate 10mg dosing for pediatric safety
✅ Eliminates DEG/EG contamination risk
✅ Improved stability vs. liquid formulation

Samples & Specs
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Ultraburst is an Innovative excipient platform for ODTs. Delivering the fastest disintegration time of any preformulated products on the market while maintaining best in class hardness, friability, and API loading and assorted tablet weights. Designed for direct compression, UltraBurst delivers on low manufacturing costs.

Sample UltraBurst
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SPI Pharma helps brands deliver high-quality, convenient solutions that consumers love—whether at home or on the go. Leverage these consumer-centric innovations to meet the needs of today’s health-conscious, busy market.

SPI Pharma
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