Prednisolone Delivery Platforms: Capsules and Beads Combination for a Right Timing Therapy.
Andrea CercielloGiulia AuriemmaSilvana MorelloRita P AquinoPasquale Del GaudioPaola RussoPublished in: PloS one (2016)
In this work, a platform of alginate beads loaded with Prednisolone in hypromellose/gellan gum capsules (F6/Cps) able to delay steroidal anti-inflammatory drug (SAID) release as needed for chronotherapy of rheumatoid arthritis is proposed. Rheumatoid arthritis, showing a worsening in symptoms in the morning upon waking, is a pathology that can benefit from chronotherapy. With the aim to maximize prednisolone therapeutic action allowing the right timing of glucocorticoid therapy, different engineered microparticles (gel-beads) were manufactured using prilling (laminar jet break-up) as micro-encapsulation technique and Zn-alginate as gastroresistant carrier. Starting from various feed solutions and process parameters, the effect of the variables on particles size, morphology, solid state properties and drug release was studied. The optimization of operative and prilling/ionotropic gelation variables led to microspheres with almost spherical shape and a narrow dimensional range. The feed solution with the highest alginate (2.5% w/v) amount and drug/polymer ratio (1:5 w/w) gave rise to the highest encapsulation efficiency (78.5%) as in F6 formulation. As to drug release, F6 exhibited an interesting dissolution profile, releasing about 24% of the drug in simulated gastric fluid followed by a more sustained profile in simulated intestinal fluid. #F6, acting as a gastro-resistant and delayed release formulation, was selected for in vivo studies on male Wistar rats by means of a carrageenan-induced oedema model. Finally, this efficacious formulation was used as core material for the development of a final dosage form: F6/Cps allowed to significantly reduce prednisolone release in simulated gastric fluid (12.6%) and delayed drug release up to about 390 minutes.
Keyphrases
- drug release
- drug delivery
- solid state
- rheumatoid arthritis
- cancer therapy
- wound healing
- anti inflammatory
- drug induced
- disease activity
- interstitial lung disease
- stem cells
- emergency department
- oxidative stress
- high glucose
- heavy metals
- systemic sclerosis
- ankylosing spondylitis
- molecularly imprinted
- risk assessment
- case control
- systemic lupus erythematosus
- tandem mass spectrometry
- stress induced