REVIEW: A Brief Introduction to Microencapsulation

Introduction

The containment of a  core material inside of a  small capsule is called  microencapsulation. A polymeric material coates liquid or solid substances to protect polymeric material from circumambient area1. Microcapsules size vary between 50 nm to 2 mm2. Microcapsule’s size and structure differs according to core material being solid, liquid or gas as in figure 12

Figure 1: (a) Mononuclear microcapsules carrying solid material, (b) Aggregated microcapsules carrying liquid material2.
Figure 2: Schematic presentation of a microcapsule2.

Coating material must be adhesive to the core material  in order to cover core material properly. Coating materials must work as an harmonious aid to core material in required strength, flexibility, impermeability, optical properties, and stability. Its release must be  controllable under required conditions1.

Figure 3 : Coating material examples1

Water Soluble MaterialsWater Insoluble Materials Waxes and Lipid Materials
GelatinCalcium alginateParaffin
Gum ArabicPolyethyleneCarnauba
StarchPolyamide (Nylon)Spermaceti
PolyvinylpyrrolidoneSiliconesBeeswax
Polyacrylic acidPolymethacrylateStearic acid
Carboxymethyl-celluloseCellulose nitrateGlyceryl stearates
Figure 4 : Alginate coated adipose stem cells extracted from (A) rat and (B) human3
 
Figure 5 : Confocal laser scanning microscope image of rhodamine-labeled hydrogel microcapsules4.

Method

  The microencapsulation of adipose stem cells  coating with alginate is shown in figure 6. The cross- linking solution contains calcium chloride and glucose and is buffered with HEPES. Calcium chloride provides divalent cations to alginate during cross-linking. Glucose is useful for maintaining physiological osmolality of the cross-linking solution for the  adipose stem cells. HEPES is used tomaintain pH at or below pH 7.33.

Figure 6: Schematic presentation of method used for  microencapsulation of adipose stem cells3.

The generation of hydrogel microcapsules with a microfluidic system is shown in figure 7. Oligosaccharides and  peptide–starPEG were inserted through two distinct channels. The flow rates of the oil phase and Oligosaccharides and  peptide–starPEG have been set  to get required droplet formation4.

Figure 7 : Scheme of the microfluidic system used for hydrogel microcapsule generation4.

Conclusion 

Microencapsulation can be used to encapsulate different materials therefore it is useful for treatment of different diseases that occurs in various tissues. There are various methods to make microcapsules. Microcapsule generation method must be chosen carefully according to the materials that microcapsule made out of. Microcapsules can be used to deliver drug molucules, various cell types into the targeted tissue. As technology improves, microencapsulation mehods will also improve and become more effective. 

References

1. MICROENCAPSULATION. Int J Pharm Sci Rev Res. 2010;5(2):58-62.

2.  M.N. Singh, K.S.Y. Hemant, M. Ram  and HGS. Microencapsulation: A promising technique for controlled drug delivery. Res Pharm Sci. 2010;5(2):65-77.

3.  Shirae K. Leslie , Ramsey C. Kinney , Zvi Schwartz  and BDB, Abstract. Microencapsulation of Stem Cells for Therapy. In: Vol 1479. ; 2017:225-235. doi:10.1007/978-1-4939-6364-5

4.  Wieduwild R, Krishnan S, Chwalek K, et al. Noncovalent Hydrogel Beads as Microcarriers for Cell Culture. Angew Chemie. 2015;127(13):4034-4038. doi:10.1002/ange.201411400

Leave a Reply

Your email address will not be published. Required fields are marked *

RSG-Turkey is a member of The International Society for Computational Biology (ISCB) Student Council (SC) Regional Student Groups (RSG). We are a non-profit community composed of early career researchers interested in computational biology and bioinformatics.

Contact: turkey.rsg@gmail.com

Follow us on social media!