Assessing Tablet-Sticking Propensity - Pharmaceutical Technology

Latest Issue

Latest Issue
PharmTech Europe

Assessing Tablet-Sticking Propensity
The authors designed an upper punch with a removable punch tip to determine a tablet formulation's propensity to stick by weighing the mass of powder adhered to the punch tip.

Pharmaceutical Technology
Volume 36, Issue 1, pp. 57-62


Figure 3: Sticking profiles and representative punch-tip images for blends containing various levels of ibuprofen.
Effect of ibuprofen loading on sticking. To investigate the sensitivity of the method to various concentrations of a sticky component, different levels of ibuprofen were mixed into a blend containing microcrystalline cellulose and 0.25% magnesium stearate. Figure 3 shows that the sticking propensity and the powder accumulated on the punch tips during the first 100 compressions tested increased with increasing ibuprofen concentrations. The quantitative measurements of accumulated powder were supported by visual inspection of punch tips, which showed high degrees of surface coverage at high ibuprofen concentrations. After approximately 100 compressions, the weight of adhered powder sometimes decreased suddenly or gradually. The sudden decreases in weight were attributed to the detachment of large domains of adhered powder from the punch tip after further compressions. The gradual decreases were attributed to a steady wearing of the film from the punch tip. These results highlight the unpredictable sticking behavior of suboptimal formulations containing high levels of sticky components and emphasize the potential for challenging manufacturing performance.

Figure 4: Tablet-sticking profile for 50% w/w spray-dried mannitol blends with various levels of magnesium stearate.

Figure 5: Tablet-sticking profile for 20% wt ibuprofen blends with various levels of magnesium stearate.
Effect of lubricant level on sticking. The effect of tableting lubricant was studied for blends containing either ibuprofen or spray-dried mannitol with various levels of magnesium stearate. As expected from tableting experience, the spray-dried mannitol had a lower absolute sticking propensity relative to ibuprofen. But, interestingly, opposite trends were observed for the mannitol versus the ibuprofen formulations with various lubricant levels. For the mannitol formulations, increasing proportions of lubricant decreased sticking (see Figure 4). This result suggests that the mannitol had a relatively high affinity for the metal punch surface, which is reduced by lubricant. Conversely, and perhaps counterintuitively, sticking increased for ibuprofen formulations containing high levels of lubricant (see Figure 5). This observation was previously reported using a different sticking assessment method and attributed to the reduction in the interparticle bond strength of ibuprofen and to a eutectic formation between the ibuprofen and magnesium stearate (1). Given these results, this method was able to indicate sticking behavior of sticky formulations as a function of small changes in the level of tableting lubricant.

Figure 6: Sticking profiles and representative punch-tip images for blends containing various grades of mannitol and various mannitol formulations.
Effect of mannitol grade on sticking. The sticking assessment method was also tested to determine whether sticking propensity could be detected using various grades of a single component. Figure 6 shows that after ~10 compressions, the powdered mannitol was about twice as sticky as granular mannitol. As expected, the microcrystalline cellulose did not stick to the punch surface. The higher sticking propensity of the powdered mannitol was hypothesized to result from its higher specific surface area, which increased its bonding potential to itself and the punch surface. A high number of compressions was not investigated with this method because of severe die-wall friction with the unlubricated powders. Mixing the granular mannitol at 75% w/w with microcrystalline cellulose, then further decreasing its concentration to 50% w/w and adding 1% w/w magnesium stearate significantly decreased the sticking propensity of the blend. This result demonstrates that the punch-sticking detection method can guide formulators when they optimize tableting-blend compositions and before progressing to large-scale manufacturing.


blog comments powered by Disqus
LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
| Weekly

What role should the US government play in the current Ebola outbreak?
Finance development of drugs to treat/prevent disease.
Oversee medical treatment of patients in the US.
Provide treatment for patients globally.
All of the above.
No government involvement in patient treatment or drug development.
Finance development of drugs to treat/prevent disease.
Oversee medical treatment of patients in the US.
Provide treatment for patients globally.
All of the above.
No government involvement in patient treatment or drug development.
Jim Miller Outsourcing Outlook Jim MillerOutside Looking In
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAdvances in Large-Scale Heterocyclic Synthesis
Jill Wechsler Regulatory Watch Jill Wechsler New Era for Generic Drugs
Sean Milmo European Regulatory WatchSean MilmoTackling Drug Shortages
New Congress to Tackle Health Reform, Biomedical Innovation, Tax Policy
Combination Products Challenge Biopharma Manufacturers
Seven Steps to Solving Tabletting and Tooling ProblemsStep 1: Clean
Legislators Urge Added Incentives for Ebola Drug Development
FDA Reorganization to Promote Drug Quality
Source: Pharmaceutical Technology,
Click here