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A Review of 20 Years Research Progression on Prodrug Technology in Inhaled Medications

A Review of 20 Years Research Progression on Prodrug Technology in Inhaled Medications

Lijuan Liu1, Jinghang Chen2*, Min Wang3 and Wei Li4

1Department of Pharmacy and Examination, Henan Vocational College of Nursing, Anyang, 455000, China.
2Department of Respiratory and Critical Care Medicine, The People’s Hospital of Anyang City, China.
3Department of Nursing, Henan Vocational College of Nursing, Anyang, 455000, China.
4Department of Medical Technology, Henan Vocational College of Nursing, Anyang, 455000, China.
 
*      Corresponding author: cjh16637232627@163.com

Fig. 1.

Prodrugs to improve physicochemical properties.

Fig. 2.

Prodrugs to reduce local and systemic toxicity. G4 PAMAM, Generation 4 polyamidoamine.

Fig. 3.

Esterified prodrugs to prolong lung retention.

Fig. 4.

Macromolecular prodrugs to prolong lung retention. PTX, Paclitaxel; IFN, Interferon; PEG, Polyethylene glycol; HSA, Human serum albumin; Sulfo-SMCC, Sulfosuccinimidyl 4-(N-maleimidomethyl)-cyclo-hexane-1-carboxylate.

Fig. 5.

Other prodrugs to prolong lung retention. PEGMAO950, Polyethylene glycol methacrylate.

Fig. 6.

Prodrugs for actively targeted delivery.

Fig. 7.

Biologically activated prodrugs for targeted drug release. DOX, Doxorubicin; PEI, Polyethylenimine.

Fig. 8.

Prodrugs for pulmonary delivery of peptides and pro- teins. Cys, Cysteine; Lys, Lysine; Pro, Proline; His, Histidine.

Fig. 9.

Inhaled bioprecursors.

Table I.

Marketed inhalation prodrugs.

Pakistan Journal of Zoology

October

Pakistan J. Zool., Vol. 56, Iss. 5, pp. 2001-2500

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