# Parkinson’s Disease: Conventional Pharmacotherapy, Drug Delivery Innovations, and Emerging Therapeutic Targets

**Authors:** Deepika Raina, Chirag Marwah, Siddharth Singh, Ansab Akhtar

PMC · DOI: 10.3390/brainsci16020226 · Brain Sciences · 2026-02-14

## TL;DR

This review discusses Parkinson’s disease, its treatment with current drugs, innovations in drug delivery, and new therapeutic targets for future therapies.

## Contribution

The paper provides a comprehensive overview of PD pharmacotherapy, delivery innovations, and emerging targets for future research.

## Key findings

- Current PD treatments like levodopa are limited by motor fluctuations and side effects.
- New drug delivery methods aim to improve efficacy and convenience for patients.
- Emerging therapeutic targets are being explored to address PD's underlying pathology.

## Abstract

Parkinson’s disease (PD) is a progressive neurodegenerative disorder characterized by motor symptoms (bradykinesia, rigidity, resting tremor) and a wide range of non-motor features. The core pathological process is degeneration of dopaminergic neurons in the substantia nigra pars compacta, leading to striatal dopamine deficiency, while additional neurotransmitter systems contribute to non-motor symptoms. PD is a common age-related disorder; global estimates for 2019 indicate that more than 8.5 million people were living with PD, and prevalence increases steeply with age. Current pharmacological therapy is mainly symptomatic and is centered on levodopa and other dopaminergic strategies, but treatment response can be limited by motor fluctuations, dyskinesia, and adverse effects. Therefore, formulation and delivery innovations (e.g., dispersible preparations, intestinal gel, and continuous infusion approaches) aim to stabilize drug exposure and improve convenience, especially in patients with swallowing difficulties or advanced disease. This review summarizes conventional drug classes and their dosage forms, highlights formulation-driven strategies to improve efficacy and tolerability, and outlines emerging pathways and targets being explored for future therapies.

## Linked entities

- **Chemicals:** levodopa (PubChem CID 6047)
- **Diseases:** Parkinson’s disease (MONDO:0005180)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, PRKN (parkin RBR E3 ubiquitin protein ligase) [NCBI Gene 5071] {aka AR-JP, LPRS2, PARK2, PDJ}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, PPFIA1 (PPFI scaffold protein A1) [NCBI Gene 8500] {aka LIP.1, LIP1, LIPRIN}, GSDMA (gasdermin A) [NCBI Gene 284110] {aka FKSG9, GSDM, GSDM1}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, PRRT2 (proline rich transmembrane protein 2) [NCBI Gene 112476] {aka BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA}, PINK1 (PTEN induced kinase 1) [NCBI Gene 65018] {aka BRPK, PARK6}, TH (tyrosine hydroxylase) [NCBI Gene 7054] {aka DYT14, DYT5b, TYH}, NTF3 (neurotrophin 3) [NCBI Gene 4908] {aka HDNF, NGF-2, NGF2, NT-3, NT3}, CASP1 (caspase 1) [NCBI Gene 834] {aka ICE, IL1BC, P45}, MAOB (monoamine oxidase B) [NCBI Gene 4129], GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, SNCA (synuclein alpha) [NCBI Gene 6622] {aka NACP, PARK1, PARK4, PD1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, COMT (catechol-O-methyltransferase) [NCBI Gene 1312] {aka HEL-S-98n}, GDNF (glial cell derived neurotrophic factor) [NCBI Gene 2668] {aka ATF, ATF1, ATF2, HFB1-GDNF, HSCR3}, GSDMD (gasdermin D) [NCBI Gene 79792] {aka DF5L, DFNA5L, FKSG10, GSDMDC1}, DDC (dopa decarboxylase) [NCBI Gene 1644] {aka AADC}, YAP1 (Yes1 associated transcriptional regulator) [NCBI Gene 10413] {aka COB1, YAP, YAP-1, YAP2, YAP65, YKI}
- **Diseases:** sleep disturbance (MESH:D012893), blurred vision (MESH:D014786), bradykinesia (MESH:D018476), resting tremor (MESH:D014202), muscle stiffness (MESH:D019042), Idiopathic Parkinsonism (MESH:D010300), mitochondrial dysfunction (MESH:D028361), skin reaction (MESH:D012871), injury (MESH:D014947), neurodegeneration (MESH:D019636), Inflammation (MESH:D007249), dopamine deficiency (MESH:C567730), melanoma (MESH:D008545), dysphagia (MESH:D003680), postural instability (MESH:D054972), motor abnormalities (MESH:D000014), traumatic brain injury (MESH:D000070642), toxicity (MESH:D064420), ptosis (MESH:C564553), Neuroinflammation (MESH:D000090862), anxiety (MESH:D001007), Alzheimer's disease (MESH:D000544), irritation (MESH:D001523), Basal ganglion degeneration (MESH:D000088282), gastrointestinal and psychiatric complications (MESH:D005767), vascular lesions (MESH:D014652), fatigue (MESH:D005221), slowing (MESH:D012897), akinesia (MESH:C537921), dementia (MESH:D003704), liver dysfunction (MESH:D017093), involuntary movements (MESH:D020820), Parkinsonism (MESH:D010302), constipation (MESH:D003248), Dopaminergic degeneration (MESH:D009410), dry mouth (MESH:D014987), stomach (MESH:D013272), gait disturbance (MESH:D020233), dyskinesia (MESH:D004409), nausea (MESH:D009325), cognitive impairment (MESH:D003072), dopaminergic (MESH:D009422), itching (MESH:D011537), extrapyramidal motor disorder (MESH:D001480), vomiting (MESH:D014839), age-related disorder (MESH:D008569), gastritis (MESH:D005756), rigidity (MESH:D009127), fever (MESH:D005334), ZI (MESH:D006562)
- **Chemicals:** caffeine (MESH:D002110), sodium (MESH:D012964), oxygen (MESH:D010100), tolcapone (MESH:D000077867), Amantadine (MESH:D000547), Fe3+ (-), hydrogen peroxide (MESH:D006861), Inosine (MESH:D007288), ethanolamine (MESH:D019856), L-DOPA (MESH:D007980), Opicapone (MESH:C549349), DOPA (MESH:D004295), ester (MESH:D004952), diphenhydramine (MESH:D004155), 1-methyl-4-phenylpyridinium (MESH:D015655), Duodopa (MESH:C009265), CoQ10 (MESH:C024989), apomorphine (MESH:D001058), Carbidopa (MESH:D002230), Urate (MESH:D014527), procyclidine (MESH:D011352), DA (MESH:C025953), 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MESH:D015632), lipid (MESH:D008055), Iron (MESH:D007501), entacapone (MESH:C071192), purine (MESH:C030985), OH- (MESH:C031356), ACh (MESH:D000109), amide (MESH:D000577), ATP (MESH:D000255), water (MESH:D014867), glutathione (MESH:D005978), 18F-dopa (MESH:C043437), rasagiline (MESH:C031967), selegiline (MESH:D012642), benserazide (MESH:D001545), nitric oxide (MESH:D009569), short-chain fatty acids (MESH:D005232), Safinamide (MESH:C092797), ROS (MESH:D017382), Rotigotine (MESH:C047508), GABA (MESH:D005680), Dopamine (MESH:D004298), kynurenine (MESH:D007737), copper (MESH:D003300), tryptophan (MESH:D014364), trihexyphenidyl (MESH:D014282), glutamate (MESH:D018698), benztropine (MESH:D001590)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## References

109 references — full list in the complete paper: https://tomesphere.com/paper/PMC12939244/full.md

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Source: https://tomesphere.com/paper/PMC12939244